ID
36653
Beschreibung
Study ID: 102970 Clinical Study ID: 102970 Study Title: A 52-week Efficacy and Safety Study to Compare the Effect of Three Dosage Strengths of Fluticasone Furoate/GW642444 Inhalation Powder With GW642444 on the Annual Rate of Exacerbations in Subjects With Chronic Obstructive Pulmonary Disease (COPD) Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: NCT01017952 Sponsor: GlaxoSmithKline Collaborators: N/A Phase: Phase 3 Study Recruitment Status: Completed Generic Name: GW642444 Inhalation Powder; FF/GW642444 Inhalation Powder Trade Name: Fluticasone Furoate;Fluticasone Propionate;Fluticasone Propionate/Salmeterol;Salmeterol;Vilanterol Study Indication: Pulmonary Disease, Chronic Obstructive
Stichworte
Versionen (2)
- 25.02.19 25.02.19 -
- 28.05.19 28.05.19 -
Rechteinhaber
GlaxoSmithKline
Hochgeladen am
28. Mai 2019
DOI
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Lizenz
Creative Commons BY-NC 3.0
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Effect of Fluticasone Furoate/GW642444 Inhalation Powder With GW642444 on Annual Rate of Exacerbations in Subjects with COPD 102970
LOGS
- StudyEvent: ODM
Beschreibung
Non-Serious Adverse Event
Alias
- UMLS CUI-1
- C1518404
Beschreibung
Non-serious Adverse Event
Datentyp
text
Alias
- UMLS CUI [1]
- C1518404
Beschreibung
Non-serious Adverse Event, Start Date
Datentyp
date
Alias
- UMLS CUI [1,1]
- C1518404
- UMLS CUI [1,2]
- C0808070
Beschreibung
Non-serious Adverse Event, Adverse Event Outcome
Datentyp
text
Alias
- UMLS CUI [1,1]
- C1518404
- UMLS CUI [1,2]
- C1705586
Beschreibung
Non-serious Adverse Event, End Date
Datentyp
date
Alias
- UMLS CUI [1,1]
- C1518404
- UMLS CUI [1,2]
- C0806020
Beschreibung
Non-serious Adverse Event, End Date
Datentyp
date
Alias
- UMLS CUI [1,1]
- C1518404
- UMLS CUI [1,2]
- C0806020
Beschreibung
Non-serious Adverse Event, Frequencies
Datentyp
text
Alias
- UMLS CUI [1,1]
- C1518404
- UMLS CUI [1,2]
- C0439603
Beschreibung
Non-serious Adverse Event, Severity of Adverse Event
Datentyp
text
Alias
- UMLS CUI [1,1]
- C1518404
- UMLS CUI [1,2]
- C1710066
Beschreibung
Non-serious Adverse Event, Action Taken with Study Treatment
Datentyp
text
Alias
- UMLS CUI [1,1]
- C1518404
- UMLS CUI [1,2]
- C1704758
Beschreibung
Non-serious Adverse Event, Withdrawal by Subject
Datentyp
boolean
Alias
- UMLS CUI [1,1]
- C1518404
- UMLS CUI [1,2]
- C1710677
Beschreibung
Non-serious Adverse Event, Investigational New Drugs, Relationships
Datentyp
boolean
Alias
- UMLS CUI [1,1]
- C1518404
- UMLS CUI [1,2]
- C0013230
- UMLS CUI [1,3]
- C0439849
Beschreibung
Serious Adverse Events
Alias
- UMLS CUI-1
- C1519255
Beschreibung
Serious Adverse Event, Experimental drug, Initiation
Datentyp
boolean
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C0304229
- UMLS CUI [1,3]
- C1704686
Beschreibung
Serious Adverse Event
Datentyp
text
Alias
- UMLS CUI [1]
- C1519255
Beschreibung
Serious Adverse Event, Start Date
Datentyp
date
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C0808070
Beschreibung
Serious Adverse Event, Adverse Event Outcome
Datentyp
text
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C1705586
Beschreibung
Serious Adverse Event, End Date
Datentyp
date
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C0806020
Beschreibung
Serious Adverse Event, End Date
Datentyp
date
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C0806020
Beschreibung
Serious Adverse Event, End Date
Datentyp
date
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C0806020
Beschreibung
Serious Adverse Event, Severity of Adverse Event
Datentyp
text
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C1710066
Beschreibung
Serious Adverse Event, Action Taken with Study Treatment
Datentyp
text
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C1704758
Beschreibung
Serious Adverse Event, Withdrawal by Subject
Datentyp
boolean
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C1710677
Beschreibung
Serious Adverse Event, Investigational New Drugs, Relationships
Datentyp
boolean
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C0013230
- UMLS CUI [1,3]
- C0439849
Beschreibung
Serious Adverse Event, Subject Study Participation Status, Relationships
Datentyp
boolean
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C2348568
- UMLS CUI [1,3]
- C0439849
Beschreibung
Serious Adverse Event, Start Date, Start time
Datentyp
datetime
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C0808070
- UMLS CUI [1,3]
- C1301880
Beschreibung
Serious Adverse Event, Symptom intensity
Datentyp
text
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C0518690
Beschreibung
Serious Adverse Event, Adverse Event Grade Code
Datentyp
text
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C2985911
Beschreibung
Serious Adverse Event, Symptom intensity, Adverse Event Grade Code
Datentyp
text
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C0518690
- UMLS CUI [1,3]
- C2985911
Beschreibung
Serious Adverse Event, Seriousness of Adverse Event
Datentyp
text
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C1710056
Beschreibung
Serious Adverse Event, Concomitant Agent, Medication name
Datentyp
text
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C2347852
- UMLS CUI [1,3]
- C2360065
Beschreibung
Serious Adverse Event, Concomitant Agent, Dosage
Datentyp
text
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C2347852
- UMLS CUI [1,3]
- C0178602
Beschreibung
Serious Adverse Event, Concomitant Agent, Unit
Datentyp
text
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C2347852
- UMLS CUI [1,3]
- C0439148
Beschreibung
Serious Adverse Event, Concomitant Agent, Frequencies
Datentyp
text
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C2347852
- UMLS CUI [1,3]
- C0439603
Beschreibung
Serious Adverse Event, Concomitant Agent, Drug Administration Routes
Datentyp
text
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C2347852
- UMLS CUI [1,3]
- C0013153
Beschreibung
Serious Adverse Event, Concomitant Medication Start Date
Datentyp
date
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C2826734
Beschreibung
Serious Adverse Event, Concomitant Medication Ongoing
Datentyp
boolean
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C2826666
Beschreibung
Serious Adverse Event, Concomitant Medication End Date
Datentyp
date
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C2826744
Beschreibung
Serious Adverse Event, Concomitant Agent, Indication
Datentyp
text
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C2347852
- UMLS CUI [1,3]
- C0392360
Beschreibung
Serious Adverse Event, Concomitant Agent, Type
Datentyp
text
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C2347852
- UMLS CUI [1,3]
- C0332307
Beschreibung
Serious Adverse Event, Disease
Datentyp
text
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C0012634
Beschreibung
Serious Adverse Event, Disease, Start Date
Datentyp
date
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C0012634
- UMLS CUI [1,3]
- C0808070
Beschreibung
Serious Adverse Event, Disease, Continuous
Datentyp
text
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C0012634
- UMLS CUI [1,3]
- C0549178
Beschreibung
Serious Adverse Event, Disease, End Date
Datentyp
date
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C0012634
- UMLS CUI [1,3]
- C0806020
Beschreibung
Serious Adverse Event, Diagnostic procedure, Test Name
Datentyp
text
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C0430022
- UMLS CUI [1,3]
- C2826273
Beschreibung
Serious Adverse Event, Diagnostic procedure, Date in time
Datentyp
date
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C0430022
- UMLS CUI [1,3]
- C0011008
Beschreibung
Serious Adverse Event, Diagnostic procedure, Result
Datentyp
text
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C0430022
- UMLS CUI [1,3]
- C1274040
Beschreibung
Serious Adverse Event, Diagnostic procedure, Unit of Measure
Datentyp
text
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C0430022
- UMLS CUI [1,3]
- C1519795
Beschreibung
Serious Adverse Event, Diagnostic procedure, Normal Range, Low
Datentyp
text
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C0430022
- UMLS CUI [1,3]
- C0086715
- UMLS CUI [1,4]
- C0205251
Beschreibung
Serious Adverse Event, Diagnostic procedure, Normal Range, High
Datentyp
text
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C0430022
- UMLS CUI [1,3]
- C0086715
- UMLS CUI [1,4]
- C0205250
Beschreibung
Serious Adverse Event, Diagnostic procedure, Result, Relevance
Datentyp
text
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C0430022
- UMLS CUI [1,3]
- C1274040
- UMLS CUI [1,4]
- C2347946
Beschreibung
Serious Adverse Event, Experimental drug, Causations
Datentyp
text
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C0304229
- UMLS CUI [1,3]
- C0085978
Beschreibung
Serious Adverse Event, Experimental drug
Datentyp
text
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C0304229
Beschreibung
Serious Adverse Event, Experimental drug, Start Date
Datentyp
date
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C0304229
- UMLS CUI [1,3]
- C0808070
Beschreibung
Serious Adverse Event, Experimental drug, End Date
Datentyp
date
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C0304229
- UMLS CUI [1,3]
- C0806020
Beschreibung
Serious Adverse Event, Experimental drug
Datentyp
text
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C0304229
Beschreibung
Serious Adverse Event, Experimental drug, Medication dose
Datentyp
text
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C0304229
- UMLS CUI [1,3]
- C3174092
Beschreibung
Serious Adverse Event, Experimental drug, Cumulative Dose
Datentyp
text
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C0304229
- UMLS CUI [1,3]
- C2986497
Beschreibung
Serious Adverse Event, Comment
Datentyp
text
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C0947611
Beschreibung
COPD Exacerbations
Alias
- UMLS CUI-1
- C0740304
Beschreibung
COPD exacerbation, Start Date
Datentyp
date
Alias
- UMLS CUI [1,1]
- C0740304
- UMLS CUI [1,2]
- C0808070
Beschreibung
COPD exacerbation, Patient Outcome
Datentyp
text
Alias
- UMLS CUI [1,1]
- C0740304
- UMLS CUI [1,2]
- C1547647
Beschreibung
COPD exacerbation, Recovered or Resolved, End Date
Datentyp
date
Alias
- UMLS CUI [1,1]
- C0740304
- UMLS CUI [1,2]
- C1709863
- UMLS CUI [1,3]
- C0806020
Beschreibung
COPD exacerbation, Fatal, End Date
Datentyp
date
Alias
- UMLS CUI [1,1]
- C0740304
- UMLS CUI [1,2]
- C1302234
- UMLS CUI [1,3]
- C0806020
Beschreibung
COPD exaverbation, Severities
Datentyp
text
Alias
- UMLS CUI [1,1]
- C0740304
- UMLS CUI [1,2]
- C0439793
Beschreibung
COPD exacerbation, Withdraw
Datentyp
boolean
Alias
- UMLS CUI [1,1]
- C0740304
- UMLS CUI [1,2]
- C2349954
Beschreibung
COPD exacerbation, Causations
Datentyp
text
Alias
- UMLS CUI [1,1]
- C0740304
- UMLS CUI [1,2]
- C0085978
Beschreibung
COPD exacerbation, Adrenal Cortex Hormones
Datentyp
boolean
Alias
- UMLS CUI [1,1]
- C0740304
- UMLS CUI [1,2]
- C0001617
Beschreibung
COPD exacerbation, Antibiotics
Datentyp
boolean
Alias
- UMLS CUI [1,1]
- C0740304
- UMLS CUI [1,2]
- C0003232
Beschreibung
COPD exacerbation, Hospitalization
Datentyp
boolean
Alias
- UMLS CUI [1,1]
- C0740304
- UMLS CUI [1,2]
- C0019993
Beschreibung
COPD exacerbation, Rescue remedy, Changed status
Datentyp
boolean
Alias
- UMLS CUI [1,1]
- C0740304
- UMLS CUI [1,2]
- C0884980
- UMLS CUI [1,3]
- C0443172
Beschreibung
COPD exacerbation, Plain chest X-ray
Datentyp
boolean
Alias
- UMLS CUI [1,1]
- C0740304
- UMLS CUI [1,2]
- C0039985
Beschreibung
COPD exacerbation, Home care of patient, Count of entities
Datentyp
integer
Alias
- UMLS CUI [1,1]
- C0740304
- UMLS CUI [1,2]
- C0204977
- UMLS CUI [1,3]
- C0449788
Beschreibung
COPD exacerbation, Physicisn, Visit, Count of entities
Datentyp
integer
Alias
- UMLS CUI [1,1]
- C0740304
- UMLS CUI [1,2]
- C0031831
- UMLS CUI [1,3]
- C0545082
- UMLS CUI [1,4]
- C0449788
Beschreibung
COPD exacerbation, Clinic Visit, Outpatient, Count of entities
Datentyp
integer
Alias
- UMLS CUI [1,1]
- C0740304
- UMLS CUI [1,2]
- C0008952
- UMLS CUI [1,3]
- C0545084
- UMLS CUI [1,4]
- C0449788
Beschreibung
COPD exacerbation, Emergency Room admission, Count of entities
Datentyp
integer
Alias
- UMLS CUI [1,1]
- C0740304
- UMLS CUI [1,2]
- C0583237
- UMLS CUI [1,3]
- C0449788
Beschreibung
COPD exacerbation, Hospitalization length of stay
Datentyp
integer
Alias
- UMLS CUI [1,1]
- C0740304
- UMLS CUI [1,2]
- C3694481
Beschreibung
COPD exacerbation, Pharmaceutical Preparations, Medication name
Datentyp
text
Alias
- UMLS CUI [1,1]
- C0740304
- UMLS CUI [1,2]
- C0013227
- UMLS CUI [1,3]
- C2360065
Beschreibung
COPD exacerbation, Pharmaceutical Preparations, Dosage
Datentyp
text
Alias
- UMLS CUI [1,1]
- C0740304
- UMLS CUI [1,2]
- C0013227
- UMLS CUI [1,3]
- C0178602
Beschreibung
COPD exacerbation, Pharmaceutical Preparations, Unit
Datentyp
text
Alias
- UMLS CUI [1,1]
- C0740304
- UMLS CUI [1,2]
- C0013227
- UMLS CUI [1,3]
- C0439148
Beschreibung
COPD exacerbation, Pharmaceutical Preparations, Frequencies
Datentyp
text
Alias
- UMLS CUI [1,1]
- C0740304
- UMLS CUI [1,2]
- C0013227
- UMLS CUI [1,3]
- C0439603
Beschreibung
COPD exacerbation, Pharmaceutical Preparations, Drug Administration Routes
Datentyp
text
Alias
- UMLS CUI [1,1]
- C0740304
- UMLS CUI [1,2]
- C0013227
- UMLS CUI [1,3]
- C0013153
Beschreibung
COPD exacerbation, Pharmaceutical Preparations, Start Date
Datentyp
date
Alias
- UMLS CUI [1,1]
- C0740304
- UMLS CUI [1,2]
- C0013227
- UMLS CUI [1,3]
- C0808070
Beschreibung
COPD exacerbation, Pharmaceutical Preparations, Previous
Datentyp
boolean
Alias
- UMLS CUI [1,1]
- C0740304
- UMLS CUI [1,2]
- C0013227
- UMLS CUI [1,3]
- C0205156
Beschreibung
COPD exacerbation, Pharmaceutical Preparations, Continuous
Datentyp
boolean
Alias
- UMLS CUI [1,1]
- C0740304
- UMLS CUI [1,2]
- C0013227
- UMLS CUI [1,3]
- C0549178
Beschreibung
COPD exacerbation, Pharmaceutical Preparations, End Date
Datentyp
date
Alias
- UMLS CUI [1,1]
- C0740304
- UMLS CUI [1,2]
- C0013227
- UMLS CUI [1,3]
- C0806020
Beschreibung
Concomitant Medications
Alias
- UMLS CUI-1
- C2347852
Beschreibung
Concomitant Agent, Medication name
Datentyp
text
Alias
- UMLS CUI [1,1]
- C2347852
- UMLS CUI [1,2]
- C2360065
Beschreibung
Concomitant Agent, Dosage
Datentyp
text
Alias
- UMLS CUI [1,1]
- C2347852
- UMLS CUI [1,2]
- C0178602
Beschreibung
Concomitant Agent, Unit
Datentyp
text
Alias
- UMLS CUI [1,1]
- C2347852
- UMLS CUI [1,2]
- C0439148
Beschreibung
Concomitant Agent, Frequencies
Datentyp
text
Alias
- UMLS CUI [1,1]
- C2347852
- UMLS CUI [1,2]
- C0439603
Beschreibung
Concomitant Agent, Drug Administration Routes
Datentyp
text
Alias
- UMLS CUI [1,1]
- C2347852
- UMLS CUI [1,2]
- C0013153
Beschreibung
Concomitant Agent, Indication
Datentyp
text
Alias
- UMLS CUI [1,1]
- C2347852
- UMLS CUI [1,2]
- C3146298
Beschreibung
Concomitant Medication Start Date
Datentyp
date
Alias
- UMLS CUI [1]
- C2826734
Beschreibung
Concomitant Medication Previous Occurrence
Datentyp
boolean
Alias
- UMLS CUI [1]
- C2826667
Beschreibung
Concomitant Medication Ongoing
Datentyp
boolean
Alias
- UMLS CUI [1]
- C2826666
Beschreibung
Concomitant Medication End Date
Datentyp
date
Alias
- UMLS CUI [1]
- C2826744
Beschreibung
Concomitant Agent, Rescue remedy
Datentyp
boolean
Alias
- UMLS CUI [1,1]
- C2347852
- UMLS CUI [1,2]
- C0884980
Beschreibung
Concomitant Agent, Type
Datentyp
text
Alias
- UMLS CUI [1,1]
- C2347852
- UMLS CUI [1,2]
- C0332307
Beschreibung
Date of Visit/Assessment
Alias
- UMLS CUI-1
- C1320303
- UMLS CUI-2
- C2985720
Beschreibung
Fracture
Alias
- UMLS CUI-1
- C0016658
Beschreibung
Fracture, Date in time
Datentyp
date
Alias
- UMLS CUI [1,1]
- C0016658
- UMLS CUI [1,2]
- C0011008
Beschreibung
Fracture, Anatomic Site, Code
Datentyp
text
Alias
- UMLS CUI [1,1]
- C0016658
- UMLS CUI [1,2]
- C1515974
- UMLS CUI [1,3]
- C0805701
Beschreibung
Fracture, Type
Datentyp
text
Alias
- UMLS CUI [1,1]
- C0016658
- UMLS CUI [1,2]
- C0332307
Beschreibung
Pharmacogenetic (PGx) Research Consent / Sample Collection
Alias
- UMLS CUI-1
- C0031325
- UMLS CUI-2
- C0021430
- UMLS CUI-3
- C0870078
Beschreibung
Pharmacogenetics, Informed Consent
Datentyp
boolean
Alias
- UMLS CUI [1,1]
- C0031325
- UMLS CUI [1,2]
- C0021430
Beschreibung
Pharmacogenetics, Informed Consent, Date in time
Datentyp
date
Alias
- UMLS CUI [1,1]
- C0031325
- UMLS CUI [1,2]
- C0021430
- UMLS CUI [1,3]
- C0011008
Beschreibung
Pharmacogenetics, Sampling
Datentyp
boolean
Alias
- UMLS CUI [1,1]
- C0031325
- UMLS CUI [1,2]
- C0870078
Beschreibung
Pharmacogenetics, Sampling, Date in time
Datentyp
date
Alias
- UMLS CUI [1,1]
- C0031325
- UMLS CUI [1,2]
- C0870078
- UMLS CUI [1,3]
- C0011008
Beschreibung
Pharmacogenetics, Sampling, Reason
Datentyp
text
Alias
- UMLS CUI [1,1]
- C0031325
- UMLS CUI [1,2]
- C0870078
- UMLS CUI [1,3]
- C0566251
Beschreibung
Double Blind Investigational Product Compliance
Alias
- UMLS CUI-1
- C0304229
- UMLS CUI-2
- C1321605
Beschreibung
Experimental drug; Containers; Identifier
Datentyp
text
Alias
- UMLS CUI [1,1]
- C0304229
- UMLS CUI [1,2]
- C0180098
- UMLS CUI [1,3]
- C0600091
Beschreibung
Experimental drug, Dispensed, Visit
Datentyp
text
Alias
- UMLS CUI [1,1]
- C0304229
- UMLS CUI [1,2]
- C1880359
- UMLS CUI [1,3]
- C0545082
Beschreibung
Experimental drug, Dispensed, Date in time
Datentyp
date
Alias
- UMLS CUI [1,1]
- C0304229
- UMLS CUI [1,2]
- C1880359
- UMLS CUI [1,3]
- C0011008
Beschreibung
Dosage, Count, Start
Datentyp
text
Alias
- UMLS CUI [1,1]
- C0178602
- UMLS CUI [1,2]
- C0750480
- UMLS CUI [1,3]
- C0452588
Beschreibung
Experimental drug, Return, Visit
Datentyp
text
Alias
- UMLS CUI [1,1]
- C0304229
- UMLS CUI [1,2]
- C0332156
- UMLS CUI [1,3]
- C0545082
Beschreibung
Experimental drug, Return, Date in time
Datentyp
date
Alias
- UMLS CUI [1,1]
- C0304229
- UMLS CUI [1,2]
- C0332156
- UMLS CUI [1,3]
- C0011008
Beschreibung
Drug Dose, Stop
Datentyp
text
Alias
- UMLS CUI [1,1]
- C0178602
- UMLS CUI [1,2]
- C2746065
Beschreibung
Open Label Diskus Taken During Run-in
Alias
- UMLS CUI-1
- C0304229
- UMLS CUI-2
- C1321605
Beschreibung
Experimental drug; Containers; Identifier
Datentyp
text
Alias
- UMLS CUI [1,1]
- C0304229
- UMLS CUI [1,2]
- C0180098
- UMLS CUI [1,3]
- C0600091
Beschreibung
Experimental drug, Dispensed, Visit
Datentyp
text
Alias
- UMLS CUI [1,1]
- C0304229
- UMLS CUI [1,2]
- C1880359
- UMLS CUI [1,3]
- C0545082
Beschreibung
Experimental drug, Dispensed, Date in time
Datentyp
date
Alias
- UMLS CUI [1,1]
- C0304229
- UMLS CUI [1,2]
- C1880359
- UMLS CUI [1,3]
- C0011008
Beschreibung
Dosage, Count, Start
Datentyp
text
Alias
- UMLS CUI [1,1]
- C0178602
- UMLS CUI [1,2]
- C0750480
- UMLS CUI [1,3]
- C0452588
Beschreibung
Experimental drug, Return, Visit
Datentyp
text
Alias
- UMLS CUI [1,1]
- C0304229
- UMLS CUI [1,2]
- C0332156
- UMLS CUI [1,3]
- C0545082
Beschreibung
Experimental drug, Return, Date in time
Datentyp
date
Alias
- UMLS CUI [1,1]
- C0304229
- UMLS CUI [1,2]
- C0332156
- UMLS CUI [1,3]
- C0011008
Beschreibung
Drug Dose, Stop
Datentyp
text
Alias
- UMLS CUI [1,1]
- C0178602
- UMLS CUI [1,2]
- C2746065
Beschreibung
IP Device Malfunction
Alias
- UMLS CUI-1
- C3898691
- UMLS CUI-2
- C0086138
Beschreibung
Investigational Medicinal Product Documentation, Identifier
Datentyp
integer
Alias
- UMLS CUI [1,1]
- C3898691
- UMLS CUI [1,2]
- C0600091
Beschreibung
Medical Device Failure or Malfunction; Indication of (contextual qualifier)
Datentyp
text
Alias
- UMLS CUI [1,1]
- C1881681
- UMLS CUI [1,2]
- C0392360
Beschreibung
Chest X-Ray
Alias
- UMLS CUI-1
- C0039985
Beschreibung
Plain chest X-ray, Date in time
Datentyp
date
Alias
- UMLS CUI [1,1]
- C0039985
- UMLS CUI [1,2]
- C0011008
Beschreibung
x-ray of chest: pulmonary infiltrate
Datentyp
text
Alias
- UMLS CUI [1]
- C2073654
Beschreibung
Plain chest X-ray, Pulmonary infiltrate, Bilateral, Unilateral
Datentyp
text
Alias
- UMLS CUI [1,1]
- C0039985
- UMLS CUI [1,2]
- C0235896
- UMLS CUI [1,3]
- C0238767
- UMLS CUI [1,4]
- C0205092
Beschreibung
Plain chest X-ray, Pulmonary infiltrate, Characterization
Datentyp
text
Alias
- UMLS CUI [1,1]
- C0039985
- UMLS CUI [1,2]
- C0235896
- UMLS CUI [1,3]
- C1880022
Beschreibung
Plain chest X-ray, Pulmonary infiltrate, Structure of right upper lobe of lung
Datentyp
text
Alias
- UMLS CUI [1,1]
- C0039985
- UMLS CUI [1,2]
- C0235896
- UMLS CUI [1,3]
- C1261074
Beschreibung
Plain chest X-ray, Pulmonary infiltrate, Structure of middle lobe of lung
Datentyp
text
Alias
- UMLS CUI [1,1]
- C0039985
- UMLS CUI [1,2]
- C0235896
- UMLS CUI [1,3]
- C0225757
Beschreibung
Plain chest X-ray, Pulmonary infiltrate, Structure of right lower lobe of lung
Datentyp
text
Alias
- UMLS CUI [1,1]
- C0039985
- UMLS CUI [1,2]
- C0235896
- UMLS CUI [1,3]
- C1261075
Beschreibung
Plain chest X-ray, Pulmonary infiltrate, Structure of left upper lobe of lung
Datentyp
text
Alias
- UMLS CUI [1,1]
- C0039985
- UMLS CUI [1,2]
- C0235896
- UMLS CUI [1,3]
- C1261076
Beschreibung
Plain chest X-ray, Pulmonary infiltrate, Lingula of left lung
Datentyp
text
Alias
- UMLS CUI [1,1]
- C0039985
- UMLS CUI [1,2]
- C0235896
- UMLS CUI [1,3]
- C0225740
Beschreibung
Plain chest X-ray, Pulmonary infiltrate, Structure of left lower lobe of lung
Datentyp
text
Alias
- UMLS CUI [1,1]
- C0039985
- UMLS CUI [1,2]
- C0235896
- UMLS CUI [1,3]
- C1261077
Beschreibung
Plain chest X-ray, Pleural effusion disorder
Datentyp
text
Alias
- UMLS CUI [1,1]
- C0039985
- UMLS CUI [1,2]
- C0032227
- UMLS CUI [1,3]
- C0450429
Beschreibung
Plain chest X-ray, Pleural effusion disorder, Location
Datentyp
text
Alias
- UMLS CUI [1,1]
- C0039985
- UMLS CUI [1,2]
- C0032227
- UMLS CUI [1,3]
- C0450429
Beschreibung
Plain chest X-ray, Atelectasis
Datentyp
text
Alias
- UMLS CUI [1,1]
- C0039985
- UMLS CUI [1,2]
- C0004144
Beschreibung
Plain chest X-ray, Lung mass
Datentyp
text
Alias
- UMLS CUI [1,1]
- C0039985
- UMLS CUI [1,2]
- C0149726
Beschreibung
Plain chest X-ray, Cardiomegaly
Datentyp
text
Alias
- UMLS CUI [1,1]
- C0039985
- UMLS CUI [1,2]
- C0018800
Beschreibung
Plain chest X-ray, Pulmonary Edema
Datentyp
text
Alias
- UMLS CUI [1,1]
- C0039985
- UMLS CUI [1,2]
- C0034063
Beschreibung
Plain chest X-ray, Comment
Datentyp
text
Alias
- UMLS CUI [1,1]
- C0039985
- UMLS CUI [1,2]
- C0947611
Beschreibung
Pneumonia Assessment
Alias
- UMLS CUI-1
- C0032285
- UMLS CUI-2
- C0220825
Beschreibung
Pneumonia, Start Date
Datentyp
date
Alias
- UMLS CUI [1,1]
- C0032285
- UMLS CUI [1,2]
- C0808070
Beschreibung
Pneumonia, Coughing, Level
Datentyp
text
Alias
- UMLS CUI [1,1]
- C0032285
- UMLS CUI [1,2]
- C0010200
- UMLS CUI [1,3]
- C2946261
Beschreibung
Pneumonia, Purulent sputum
Datentyp
text
Alias
- UMLS CUI [1,1]
- C0032285
- UMLS CUI [1,2]
- C0241235
Beschreibung
Pneumonia, Chest auscultation finding
Datentyp
text
Alias
- UMLS CUI [1,1]
- C0032285
- UMLS CUI [1,2]
- C0577960
Beschreibung
Pneumonia, Dyspnea
Datentyp
text
Alias
- UMLS CUI [1,1]
- C0032285
- UMLS CUI [1,2]
- C0013404
Beschreibung
Pneumonia, Blood culture
Datentyp
text
Alias
- UMLS CUI [1,1]
- C0032285
- UMLS CUI [1,2]
- C0200949
Beschreibung
Pneumonia, Blood culture, Pathogenic organism
Datentyp
text
Alias
- UMLS CUI [1,1]
- C0032285
- UMLS CUI [1,2]
- C0200949
- UMLS CUI [1,3]
- C0450254
Beschreibung
Pneumonia, Pleural effusion disorder, Location
Datentyp
text
Alias
- UMLS CUI [1,1]
- C0032285
- UMLS CUI [1,2]
- C0032227
- UMLS CUI [1,3]
- C0450429
Beschreibung
Body Temperature
Datentyp
float
Maßeinheiten
- °C
Alias
- UMLS CUI [1]
- C0005903
Beschreibung
Respiratory rate
Datentyp
integer
Maßeinheiten
- breaths/min
Alias
- UMLS CUI [1]
- C0231832
Beschreibung
Heart rate
Datentyp
integer
Maßeinheiten
- bpm
Alias
- UMLS CUI [1]
- C0018810
Beschreibung
Systolic Pressure
Datentyp
integer
Maßeinheiten
- mmHg
Alias
- UMLS CUI [1,1]
- C0871470
- UMLS CUI [1,2]
- C0522019
Beschreibung
Diastolic blood pressure
Datentyp
integer
Maßeinheiten
- mmHg
Alias
- UMLS CUI [1]
- C0428883
Beschreibung
Pneumonia, Hypoxemia
Datentyp
text
Alias
- UMLS CUI [1,1]
- C0032285
- UMLS CUI [1,2]
- C0700292
Beschreibung
Pneumonia, White blood cell count procedure
Datentyp
text
Alias
- UMLS CUI [1,1]
- C0032285
- UMLS CUI [1,2]
- C0023508
Beschreibung
Pneumonia, Inpatient
Datentyp
text
Alias
- UMLS CUI [1,1]
- C0032285
- UMLS CUI [1,2]
- C0021562
Beschreibung
Pneumonia, X-Ray confirmed
Datentyp
boolean
Alias
- UMLS CUI [1]
- C3843750
Beschreibung
Pneumonia, Hospitalization
Datentyp
boolean
Alias
- UMLS CUI [1,1]
- C0032285
- UMLS CUI [1,2]
- C0019993
Beschreibung
Pneumonia, Cessation of life
Datentyp
boolean
Alias
- UMLS CUI [1,1]
- C0032285
- UMLS CUI [1,2]
- C0011065
Beschreibung
Log Status
Alias
- UMLS CUI-1
- C1708728
- UMLS CUI-2
- C0449438
Beschreibung
Concomitant Agent, During, Clinical Trials
Datentyp
boolean
Alias
- UMLS CUI [1,1]
- C2347852
- UMLS CUI [1,2]
- C0347984
- UMLS CUI [1,3]
- C0008976
Beschreibung
Non-serious Adverse Event
Datentyp
boolean
Alias
- UMLS CUI [1]
- C1518404
Beschreibung
COPD exacerbation
Datentyp
boolean
Alias
- UMLS CUI [1]
- C0740304
Beschreibung
Pneumonia
Datentyp
boolean
Alias
- UMLS CUI [1]
- C0032285
Beschreibung
Fracture
Datentyp
boolean
Alias
- UMLS CUI [1]
- C0016658
Beschreibung
Dry Powder Inhaler Device, Device Failure
Datentyp
text
Alias
- UMLS CUI [1,1]
- C1967611
- UMLS CUI [1,2]
- C0086138
Beschreibung
SAE Status
Alias
- UMLS CUI-1
- C1519255
- UMLS CUI-2
- C0449438
Beschreibung
Subject Status
Alias
- UMLS CUI-1
- C2348568
Ähnliche Modelle
LOGS
- StudyEvent: ODM
C0808070 (UMLS CUI [1,2])
C1705586 (UMLS CUI [1,2])
C0806020 (UMLS CUI [1,2])
C0806020 (UMLS CUI [1,2])
C0439603 (UMLS CUI [1,2])
C1710066 (UMLS CUI [1,2])
C1704758 (UMLS CUI [1,2])
C1710677 (UMLS CUI [1,2])
C0013230 (UMLS CUI [1,2])
C0439849 (UMLS CUI [1,3])
C0304229 (UMLS CUI [1,2])
C1704686 (UMLS CUI [1,3])
C0808070 (UMLS CUI [1,2])
C1705586 (UMLS CUI [1,2])
C0806020 (UMLS CUI [1,2])
C0806020 (UMLS CUI [1,2])
C0806020 (UMLS CUI [1,2])
C1710066 (UMLS CUI [1,2])
C1704758 (UMLS CUI [1,2])
C1710677 (UMLS CUI [1,2])
C0013230 (UMLS CUI [1,2])
C0439849 (UMLS CUI [1,3])
C2348568 (UMLS CUI [1,2])
C0439849 (UMLS CUI [1,3])
C0808070 (UMLS CUI [1,2])
C1301880 (UMLS CUI [1,3])
C0518690 (UMLS CUI [1,2])
C2985911 (UMLS CUI [1,2])
C0518690 (UMLS CUI [1,2])
C2985911 (UMLS CUI [1,3])
C1710056 (UMLS CUI [1,2])
C2347852 (UMLS CUI [1,2])
C2360065 (UMLS CUI [1,3])
C2347852 (UMLS CUI [1,2])
C0178602 (UMLS CUI [1,3])
C2347852 (UMLS CUI [1,2])
C0439148 (UMLS CUI [1,3])
C2347852 (UMLS CUI [1,2])
C0439603 (UMLS CUI [1,3])
C2347852 (UMLS CUI [1,2])
C0013153 (UMLS CUI [1,3])
C2826734 (UMLS CUI [1,2])
C2826666 (UMLS CUI [1,2])
C2826744 (UMLS CUI [1,2])
C2347852 (UMLS CUI [1,2])
C0392360 (UMLS CUI [1,3])
C2347852 (UMLS CUI [1,2])
C0332307 (UMLS CUI [1,3])
C0012634 (UMLS CUI [1,2])
C0012634 (UMLS CUI [1,2])
C0808070 (UMLS CUI [1,3])
C0012634 (UMLS CUI [1,2])
C0549178 (UMLS CUI [1,3])
C0012634 (UMLS CUI [1,2])
C0806020 (UMLS CUI [1,3])
C0430022 (UMLS CUI [1,2])
C2826273 (UMLS CUI [1,3])
C0430022 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,3])
C0430022 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C0430022 (UMLS CUI [1,2])
C1519795 (UMLS CUI [1,3])
C0430022 (UMLS CUI [1,2])
C0086715 (UMLS CUI [1,3])
C0205251 (UMLS CUI [1,4])
C0430022 (UMLS CUI [1,2])
C0086715 (UMLS CUI [1,3])
C0205250 (UMLS CUI [1,4])
C0430022 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C2347946 (UMLS CUI [1,4])
C0304229 (UMLS CUI [1,2])
C0085978 (UMLS CUI [1,3])
C0304229 (UMLS CUI [1,2])
C0304229 (UMLS CUI [1,2])
C0808070 (UMLS CUI [1,3])
C0304229 (UMLS CUI [1,2])
C0806020 (UMLS CUI [1,3])
C0304229 (UMLS CUI [1,2])
C0304229 (UMLS CUI [1,2])
C3174092 (UMLS CUI [1,3])
C0304229 (UMLS CUI [1,2])
C2986497 (UMLS CUI [1,3])
C0947611 (UMLS CUI [1,2])
C0808070 (UMLS CUI [1,2])
C1547647 (UMLS CUI [1,2])
C1709863 (UMLS CUI [1,2])
C0806020 (UMLS CUI [1,3])
C1302234 (UMLS CUI [1,2])
C0806020 (UMLS CUI [1,3])
C0439793 (UMLS CUI [1,2])
C2349954 (UMLS CUI [1,2])
C0085978 (UMLS CUI [1,2])
C0001617 (UMLS CUI [1,2])
C0003232 (UMLS CUI [1,2])
C0019993 (UMLS CUI [1,2])
C0884980 (UMLS CUI [1,2])
C0443172 (UMLS CUI [1,3])
C0039985 (UMLS CUI [1,2])
C0204977 (UMLS CUI [1,2])
C0449788 (UMLS CUI [1,3])
C0031831 (UMLS CUI [1,2])
C0545082 (UMLS CUI [1,3])
C0449788 (UMLS CUI [1,4])
C0008952 (UMLS CUI [1,2])
C0545084 (UMLS CUI [1,3])
C0449788 (UMLS CUI [1,4])
C0583237 (UMLS CUI [1,2])
C0449788 (UMLS CUI [1,3])
C3694481 (UMLS CUI [1,2])
C0013227 (UMLS CUI [1,2])
C2360065 (UMLS CUI [1,3])
C0013227 (UMLS CUI [1,2])
C0178602 (UMLS CUI [1,3])
C0013227 (UMLS CUI [1,2])
C0439148 (UMLS CUI [1,3])
C0013227 (UMLS CUI [1,2])
C0439603 (UMLS CUI [1,3])
C0013227 (UMLS CUI [1,2])
C0013153 (UMLS CUI [1,3])
C0013227 (UMLS CUI [1,2])
C0808070 (UMLS CUI [1,3])
C0013227 (UMLS CUI [1,2])
C0205156 (UMLS CUI [1,3])
C0013227 (UMLS CUI [1,2])
C0549178 (UMLS CUI [1,3])
C0013227 (UMLS CUI [1,2])
C0806020 (UMLS CUI [1,3])
C2360065 (UMLS CUI [1,2])
C0178602 (UMLS CUI [1,2])
C0439148 (UMLS CUI [1,2])
C0439603 (UMLS CUI [1,2])
C0013153 (UMLS CUI [1,2])
C3146298 (UMLS CUI [1,2])
C0884980 (UMLS CUI [1,2])
C0332307 (UMLS CUI [1,2])
C2985720 (UMLS CUI-2)
C2985720 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,2])
C1515974 (UMLS CUI [1,2])
C0805701 (UMLS CUI [1,3])
C0021430 (UMLS CUI-2)
C0870078 (UMLS CUI-3)
C0021430 (UMLS CUI [1,2])
C0021430 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,3])
C0870078 (UMLS CUI [1,2])
C0870078 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,3])
C0870078 (UMLS CUI [1,2])
C0566251 (UMLS CUI [1,3])
C1321605 (UMLS CUI-2)
C0180098 (UMLS CUI [1,2])
C0600091 (UMLS CUI [1,3])
C1880359 (UMLS CUI [1,2])
C0545082 (UMLS CUI [1,3])
C1880359 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,3])
C0750480 (UMLS CUI [1,2])
C0452588 (UMLS CUI [1,3])
C0332156 (UMLS CUI [1,2])
C0545082 (UMLS CUI [1,3])
C0332156 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,3])
C2746065 (UMLS CUI [1,2])
C1321605 (UMLS CUI-2)
C0180098 (UMLS CUI [1,2])
C0600091 (UMLS CUI [1,3])
C1880359 (UMLS CUI [1,2])
C0545082 (UMLS CUI [1,3])
C1880359 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,3])
C0750480 (UMLS CUI [1,2])
C0452588 (UMLS CUI [1,3])
C0332156 (UMLS CUI [1,2])
C0545082 (UMLS CUI [1,3])
C0332156 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,3])
C2746065 (UMLS CUI [1,2])
C0086138 (UMLS CUI-2)
C0600091 (UMLS CUI [1,2])
C0392360 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,2])
C0235896 (UMLS CUI [1,2])
C0238767 (UMLS CUI [1,3])
C0205092 (UMLS CUI [1,4])
C0235896 (UMLS CUI [1,2])
C1880022 (UMLS CUI [1,3])
C0235896 (UMLS CUI [1,2])
C1261074 (UMLS CUI [1,3])
C0235896 (UMLS CUI [1,2])
C0225757 (UMLS CUI [1,3])
C0235896 (UMLS CUI [1,2])
C1261075 (UMLS CUI [1,3])
C0235896 (UMLS CUI [1,2])
C1261076 (UMLS CUI [1,3])
C0235896 (UMLS CUI [1,2])
C0225740 (UMLS CUI [1,3])
C0235896 (UMLS CUI [1,2])
C1261077 (UMLS CUI [1,3])
C0032227 (UMLS CUI [1,2])
C0450429 (UMLS CUI [1,3])
C0032227 (UMLS CUI [1,2])
C0450429 (UMLS CUI [1,3])
C0004144 (UMLS CUI [1,2])
C0149726 (UMLS CUI [1,2])
C0018800 (UMLS CUI [1,2])
C0034063 (UMLS CUI [1,2])
C0947611 (UMLS CUI [1,2])
C0808070 (UMLS CUI [1,2])
C0010200 (UMLS CUI [1,2])
C2946261 (UMLS CUI [1,3])
C0241235 (UMLS CUI [1,2])
C0577960 (UMLS CUI [1,2])
C0200949 (UMLS CUI [1,2])
C0200949 (UMLS CUI [1,2])
C0450254 (UMLS CUI [1,3])
C0032227 (UMLS CUI [1,2])
C0450429 (UMLS CUI [1,3])
C0522019 (UMLS CUI [1,2])
C0700292 (UMLS CUI [1,2])
C0023508 (UMLS CUI [1,2])
C0021562 (UMLS CUI [1,2])
C0019993 (UMLS CUI [1,2])
C0011065 (UMLS CUI [1,2])
C0347984 (UMLS CUI [1,2])
C0008976 (UMLS CUI [1,3])
C0086138 (UMLS CUI [1,2])