ID
42267
Description
Study ID: 107671 Clinical Study ID: 107671 Study Title: EGF107671 – A Phase II Study of Lapatinib plus Topotecan or Lapatinib plus Capecitabine in the Treatment of Recurrent Brain Metastases from ErbB2-Positive Breast Cancer Following Cranial Radiotherapy Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: NCT00437073 Sponsor: GlaxoSmithKline Collaborators: N/A Phase: Phase 2 Study Recruitment Status: Completed Generic Name: N/A Trade Name: capecitabine, topotecan, lapatinib Study Indication: Neoplasms, Breast; Recurrent Brain Metastases
Mots-clés
Versions (2)
- 13/10/2020 13/10/2020 -
- 26/04/2021 26/04/2021 - Sarah Riepenhausen
Détendeur de droits
GlaxoSmithKline
Téléchargé le
26 avril 2021
DOI
Pour une demande vous connecter.
Licence
Creative Commons BY 4.0
Modèle Commentaires :
Ici, vous pouvez faire des commentaires sur le modèle. À partir des bulles de texte, vous pouvez laisser des commentaires spécifiques sur les groupes Item et les Item.
Groupe Item commentaires pour :
Item commentaires pour :
Vous devez être connecté pour pouvoir télécharger des formulaires. Veuillez vous connecter ou s’inscrire gratuitement.
Lapatinib + Topotecan or + Capecitabine in Recurrent Brain Metastases from Breast Cancer; NCT00437073
Log
- StudyEvent: ODM
Description
Log Status
Alias
- UMLS CUI-1
- C1708728
- UMLS CUI-2
- C0449438
Description
Concomitant Agent
Type de données
boolean
Alias
- UMLS CUI [1]
- C2347852
Description
Concomitant Agent, Adrenal Cortex Hormones
Type de données
boolean
Alias
- UMLS CUI [1,1]
- C2347852
- UMLS CUI [1,2]
- C0001617
Description
Non-serious Adverse Event
Type de données
boolean
Alias
- UMLS CUI [1]
- C1518404
Description
Serious Adverse Event
Type de données
boolean
Alias
- UMLS CUI [1]
- C1519255
Description
Blood product; Blood product, Supportive care
Type de données
boolean
Alias
- UMLS CUI [1]
- C0456388
- UMLS CUI [2,1]
- C0456388
- UMLS CUI [2,2]
- C0344211
Description
Collection of blood specimen for laboratory procedure, Pharmacogenetics
Type de données
boolean
Alias
- UMLS CUI [1,1]
- C0005834
- UMLS CUI [1,2]
- C0031325
Description
Non-Serious Adverse Event (AE) - Repeating Form
Alias
- UMLS CUI-1
- C1518404
Description
Non-serious Adverse Event, Sequence Number
Type de données
integer
Alias
- UMLS CUI [1,1]
- C1518404
- UMLS CUI [1,2]
- C2348184
Description
Non-serious Adverse Event
Type de données
text
Alias
- UMLS CUI [1]
- C1518404
Description
Non-serious Adverse Event, Adverse Event Modified Reported Term
Type de données
text
Alias
- UMLS CUI [1,1]
- C1518404
- UMLS CUI [1,2]
- C2826798
Description
Non-serious Adverse Event, Medical Dictionary for Regulatory Activities Terminology (MedDRA)
Type de données
text
Alias
- UMLS CUI [1,1]
- C1518404
- UMLS CUI [1,2]
- C1140263
Description
Non-serious Adverse Event, MedDRA Low Level Term Code
Type de données
text
Alias
- UMLS CUI [1,1]
- C1518404
- UMLS CUI [1,2]
- C3898442
Description
Non-serious Adverse Event, Code, Failed
Type de données
text
Alias
- UMLS CUI [1,1]
- C1518404
- UMLS CUI [1,2]
- C0805701
- UMLS CUI [1,3]
- C0231175
Description
Non-serious Adverse Event, Start DateStart Date
Type de données
date
Alias
- UMLS CUI [1,1]
- C1518404
- UMLS CUI [1,2]
- C0808070
Description
Non-serious Adverse Event, Adverse Event Outcome
Type de données
text
Alias
- UMLS CUI [1,1]
- C1518404
- UMLS CUI [1,2]
- C1705586
Description
Non-serious Adverse Event, End Date
Type de données
date
Alias
- UMLS CUI [1,1]
- C1518404
- UMLS CUI [1,2]
- C0806020
Description
Non-serious Adverse Event, Frequencies
Type de données
text
Alias
- UMLS CUI [1,1]
- C1518404
- UMLS CUI [1,2]
- C0439603
Description
Non-serious Adverse Event, Symptom intensity, Maximum
Type de données
text
Alias
- UMLS CUI [1,1]
- C1518404
- UMLS CUI [1,2]
- C0518690
- UMLS CUI [1,3]
- C0806909
Description
Non-serious Adverse Event, Grade, Maximum
Type de données
text
Alias
- UMLS CUI [1,1]
- C1518404
- UMLS CUI [1,2]
- C0441800
- UMLS CUI [1,3]
- C0806909
Description
Non-serious Adverse Event, Grade, Maximum; Non-serious Adverse Event, Symptom intensity, Maximum
Type de données
text
Alias
- UMLS CUI [1,1]
- C1518404
- UMLS CUI [1,2]
- C0441800
- UMLS CUI [1,3]
- C0806909
- UMLS CUI [2,1]
- C1518404
- UMLS CUI [2,2]
- C0518690
- UMLS CUI [2,3]
- C0806909
Description
Non-serious Adverse Event, Action Taken with Study Treatment
Type de données
text
Alias
- UMLS CUI [1,1]
- C1518404
- UMLS CUI [1,2]
- C1704758
Description
Non-serious Adverse Event, Withdraw
Type de données
boolean
Alias
- UMLS CUI [1,1]
- C1518404
- UMLS CUI [1,2]
- C2349954
Description
Non-serious Adverse Event, Relationships, Experimental drug
Type de données
boolean
Alias
- UMLS CUI [1,1]
- C1518404
- UMLS CUI [1,2]
- C0439849
- UMLS CUI [1,3]
- C0304229
Description
Non-serious Adverse Event, Duration
Type de données
time
Alias
- UMLS CUI [1,1]
- C1518404
- UMLS CUI [1,2]
- C2926735
Description
Non-serious Adverse Event, Time of onset, Time last dose
Type de données
time
Alias
- UMLS CUI [1,1]
- C1518404
- UMLS CUI [1,2]
- C0449244
- UMLS CUI [1,3]
- C0946444
Description
Serious Adverse Events (SAE) - Repeating Form
Alias
- UMLS CUI-1
- C1519255
Description
Serious Adverse Event Report, Type
Type de données
text
Alias
- UMLS CUI [1,1]
- C3897642
- UMLS CUI [1,2]
- C0332307
Description
Serious Adverse Event, Experimental drug
Type de données
boolean
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C0304229
Description
Serious Adverse Event, Sequence Number
Type de données
integer
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C2348184
Description
Serious Adverse Event
Type de données
text
Alias
- UMLS CUI [1]
- C1519255
Description
Serious Adverse Event, Adverse Event Modified Reported Term
Type de données
text
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C2826798
Description
Serious Adverse Event, Medical Dictionary for Regulatory Activities Terminology (MedDRA)
Type de données
text
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C1140263
Description
Serious Adverse Event, MedDRA Low Level Term Code
Type de données
text
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C3898442
Description
Serious Adverse Event, Code, Failed
Type de données
text
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C0805701
- UMLS CUI [1,3]
- C0231175
Description
Serious Adverse Event, Start Date
Type de données
date
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C0808070
Description
Serious Adverse Event, Adverse Event Outcome
Type de données
text
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C1705586
Description
Serious Adverse Event, End Date; Serious Adverse Event, Date of death
Type de données
date
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C0806020
- UMLS CUI [2,1]
- C1519255
- UMLS CUI [2,2]
- C1148348
Description
Serious Adverse Event, Symptom intensity, Maximum
Type de données
text
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C0518690
- UMLS CUI [1,3]
- C0806909
Description
Serious Adverse Event, Grade, Maximum
Type de données
text
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C0441800
- UMLS CUI [1,3]
- C0806909
Description
Serious Adverse Event, Grade, Maximum; Serious Adverse Event, Symptom intensity, Maximum
Type de données
text
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C0441800
- UMLS CUI [1,3]
- C0806909
- UMLS CUI [2,1]
- C1519255
- UMLS CUI [2,2]
- C0518690
- UMLS CUI [2,3]
- C0806909
Description
Serious Adverse Event, Action Taken with Study Treatment
Type de données
text
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C1704758
Description
Serious Adverse Event, Withdraw
Type de données
boolean
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C2349954
Description
Serious Adverse Event, Relationships, Experimental drug
Type de données
boolean
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C0439849
- UMLS CUI [1,3]
- C0304229
Description
Serious Adverse Event, Duration
Type de données
time
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C2926735
Description
Serious Adverse Event, Time of onset, Time last dose
Type de données
time
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C0449244
- UMLS CUI [1,3]
- C0946444
Description
Serious Adverse Event, Relationships, Study Subject Participation Status
Type de données
boolean
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C0439849
- UMLS CUI [1,3]
- C2348568
Description
Serious Adverse Event
Type de données
boolean
Alias
- UMLS CUI [1]
- C1519255
Description
Serious Adverse Event, Seriousness of Adverse Event
Type de données
text
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C1710056
Description
Serious Adverse Event, Concomitant Medication, Sequence Number
Type de données
integer
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C2347852
- UMLS CUI [1,3]
- C2348184
Description
Serious Adverse Event, Concomitant Agent, Medication name
Type de données
text
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C2347852
- UMLS CUI [1,3]
- C2360065
Description
Serious Adverse Event, Concomitant Agent, Dosage
Type de données
text
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C2347852
- UMLS CUI [1,3]
- C0178602
Description
Serious Adverse Event, Concomitant Agent, Unit of Measure
Type de données
text
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C2347852
- UMLS CUI [1,3]
- C1519795
Description
Serious Adverse Event, Concomitant Agent, Frequencies
Type de données
text
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C2347852
- UMLS CUI [1,3]
- C0439603
Description
Serious Adverse Event, Concomitant Agent, Drug Administration Routes
Type de données
text
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C2347852
- UMLS CUI [1,3]
- C0013153
Description
Serious Adverse Event, Concomitant Medication, Start Date
Type de données
date
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C2347852
- UMLS CUI [1,3]
- C0808070
Description
Serious Adverse Event, Concomitant Medication Ongoing
Type de données
boolean
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C2826666
Description
Serious Adverse Event, Concomitant Agent, End Date
Type de données
date
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C2347852
- UMLS CUI [1,3]
- C0806020
Description
Serious Adverse Event, Disease, Risk factor, Sequence Number
Type de données
integer
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C0012634
- UMLS CUI [1,3]
- C0035648
- UMLS CUI [1,4]
- C2348184
Description
Serious Adverse Event, Disease
Type de données
text
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C0012634
Description
Serious Adverse Event, Disease, Start Date
Type de données
date
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C0012634
- UMLS CUI [1,3]
- C0808070
Description
Serious Adverse Event, Disease, Continuous
Type de données
text
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C0012634
- UMLS CUI [1,3]
- C0549178
Description
Serious Adverse Event, Disease, End Date
Type de données
date
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C0012634
- UMLS CUI [1,3]
- C0806020
Description
Serious Adverse Event, Disease, Risk factor, Other
Type de données
text
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C0012634
- UMLS CUI [1,3]
- C0035648
- UMLS CUI [1,4]
- C0205394
Description
Serious Adverse Event, Diagnostic procedures, Result, Sequence Number
Type de données
integer
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C0430022
- UMLS CUI [1,3]
- C1274040
- UMLS CUI [1,4]
- C2348184
Description
Serious Adverse Event, Diagnostic procedures
Type de données
text
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C0430022
Description
Serious Adverse Event, Diagnostic procedures, Date in time
Type de données
date
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C0430022
- UMLS CUI [1,3]
- C0011008
Description
Serious Adverse Event, Diagnostic procedures, Result
Type de données
text
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C0430022
- UMLS CUI [1,3]
- C1274040
Description
Serious Adverse Event, Diagnostic procedures, Unit of Measure
Type de données
text
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C0430022
- UMLS CUI [1,3]
- C1519795
Description
Serious Adverse Event, Diagnostic procedures, Normal Range, Low
Type de données
text
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C0430022
- UMLS CUI [1,3]
- C0086715
- UMLS CUI [1,4]
- C0205251
Description
Serious Adverse Event, Diagnostic procedures, Normal Range, High
Type de données
text
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C0430022
- UMLS CUI [1,3]
- C0086715
- UMLS CUI [1,4]
- C0205250
Description
Serious Adverse Event, Diagnostic procedures, Result, Other
Type de données
text
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C0430022
- UMLS CUI [1,3]
- C1274040
- UMLS CUI [1,4]
- C0205394
Description
Serious Adverse Event, Relationships, Experimental drug
Type de données
text
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C0439849
- UMLS CUI [1,3]
- C0304229
Description
Serious Adverse Event, Comment
Type de données
text
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C0947611
Description
Concomitant Medications - Repeating Form
Alias
- UMLS CUI-1
- C2347852
Description
Concomitant Agent, Sequence Number
Type de données
integer
Alias
- UMLS CUI [1,1]
- C2347852
- UMLS CUI [1,2]
- C2348184
Description
Concomitant Agent, Medication name
Type de données
text
Alias
- UMLS CUI [1,1]
- C2347852
- UMLS CUI [1,2]
- C2360065
Description
Concomitant Medication Modified Reported Term
Type de données
text
Alias
- UMLS CUI [1]
- C2826819
Description
Concomitant Agent, Synonym
Type de données
text
Alias
- UMLS CUI [1,1]
- C2347852
- UMLS CUI [1,2]
- C0871468
Description
Concomitant Agent, Code
Type de données
text
Alias
- UMLS CUI [1,1]
- C2347852
- UMLS CUI [1,2]
- C0805701
Description
Concomitant Agent, Code, Failed
Type de données
text
Alias
- UMLS CUI [1,1]
- C2347852
- UMLS CUI [1,2]
- C0805701
- UMLS CUI [1,3]
- C0231175
Description
Concomitant Agent, Reason and justification
Type de données
text
Alias
- UMLS CUI [1,1]
- C2347852
- UMLS CUI [1,2]
- C0566251
Description
Concomitant Agent, Start Date
Type de données
date
Alias
- UMLS CUI [1,1]
- C2347852
- UMLS CUI [1,2]
- C0808070
Description
Concomitant Medication Previous Occurrence
Type de données
boolean
Alias
- UMLS CUI [1]
- C2826667
Description
Concomitant Medication Ongoing
Type de données
boolean
Alias
- UMLS CUI [1]
- C2826666
Description
Concomitant Agent, End Date
Type de données
date
Alias
- UMLS CUI [1,1]
- C2347852
- UMLS CUI [1,2]
- C0806020
Description
Corticosteroid Concomitant Medications - Repeating Form
Alias
- UMLS CUI-1
- C2347852
- UMLS CUI-2
- C0001617
Description
Concomitant Agent, Adrenal Cortex Hormones, Sequence Number
Type de données
integer
Alias
- UMLS CUI [1,1]
- C2347852
- UMLS CUI [1,2]
- C0001617
- UMLS CUI [1,3]
- C2348184
Description
Concomitant Agent, Adrenal Cortex Hormones, Medication name
Type de données
text
Alias
- UMLS CUI [1,1]
- C2347852
- UMLS CUI [1,2]
- C0001617
- UMLS CUI [1,3]
- C2360065
Description
Concomitant Medication Modified Reported Term, Adrenal Cortex Hormones
Type de données
text
Alias
- UMLS CUI [1,1]
- C2826819
- UMLS CUI [1,2]
- C0001617
Description
Concomitant Agent, Adrenal Cortex Hormones, Synonym
Type de données
text
Alias
- UMLS CUI [1,1]
- C2347852
- UMLS CUI [1,2]
- C0001617
- UMLS CUI [1,3]
- C0871468
Description
Concomitant Agent, Adrenal Cortex Hormones, Code
Type de données
text
Alias
- UMLS CUI [1,1]
- C2347852
- UMLS CUI [1,2]
- C0001617
- UMLS CUI [1,3]
- C0805701
Description
Concomitant Agent, Adrenal Cortex Hormones, Code, Failed
Type de données
text
Alias
- UMLS CUI [1,1]
- C2347852
- UMLS CUI [1,2]
- C0001617
- UMLS CUI [1,3]
- C0805701
- UMLS CUI [1,4]
- C0231175
Description
Concomitant Agent, Adrenal Cortex Hormones, Daily Dose, Total
Type de données
text
Alias
- UMLS CUI [1,1]
- C2347852
- UMLS CUI [1,2]
- C0001617
- UMLS CUI [1,3]
- C2348070
- UMLS CUI [1,4]
- C0439810
Description
Concomitant Agent, Adrenal Cortex Hormones, Unit of Measure
Type de données
text
Alias
- UMLS CUI [1,1]
- C2347852
- UMLS CUI [1,2]
- C0001617
- UMLS CUI [1,3]
- C1519795
Description
Concomitant Agent, Adrenal Cortex Hormones, Frequencies
Type de données
text
Alias
- UMLS CUI [1,1]
- C2347852
- UMLS CUI [1,2]
- C0001617
- UMLS CUI [1,3]
- C0439603
Description
Concomitant Agent,Adrenal Cortex Hormones, Drug Administration Routes
Type de données
text
Alias
- UMLS CUI [1,1]
- C2347852
- UMLS CUI [1,2]
- C0001617
- UMLS CUI [1,3]
- C0013153
Description
Concomitant Agent, Adrenal Cortex Hormones, Reason and justification
Type de données
text
Alias
- UMLS CUI [1,1]
- C2347852
- UMLS CUI [1,2]
- C0001617
- UMLS CUI [1,3]
- C0566251
Description
Concomitant Agent, Adrenal Cortex Hormones, Reason and justification
Type de données
text
Alias
- UMLS CUI [1,1]
- C2347852
- UMLS CUI [1,2]
- C0001617
- UMLS CUI [1,3]
- C0566251
Description
Concomitant Agent, Adrenal Cortex Hormones, Start Date
Type de données
date
Alias
- UMLS CUI [1,1]
- C2347852
- UMLS CUI [1,2]
- C0001617
- UMLS CUI [1,3]
- C0808070
Description
Concomitant Medication Previous Occurrence, Adrenal Cortex Hormones
Type de données
boolean
Alias
- UMLS CUI [1,1]
- C2826667
- UMLS CUI [1,2]
- C0001617
Description
Concomitant Medication Ongoing,Adrenal Cortex Hormones
Type de données
boolean
Alias
- UMLS CUI [1,1]
- C2826666
- UMLS CUI [1,2]
- C0001617
Description
Concomitant Agent, Adrenal Cortex Hormones, End Date
Type de données
date
Alias
- UMLS CUI [1,1]
- C2347852
- UMLS CUI [1,2]
- C0001617
- UMLS CUI [1,3]
- C0806020
Description
Blood Products and Blood Supportive Care Products
Alias
- UMLS CUI-1
- C0456388
- UMLS CUI-2
- C0344211
Description
Blood product, Sequence Number; Blood product, Supportive care, Sequence Number
Type de données
integer
Alias
- UMLS CUI [1,1]
- C0456388
- UMLS CUI [1,2]
- C2348184
- UMLS CUI [2,1]
- C0456388
- UMLS CUI [2,2]
- C0344211
- UMLS CUI [2,3]
- C2348184
Description
Blood product; Blood product, Supportive care
Type de données
text
Alias
- UMLS CUI [1]
- C0456388
- UMLS CUI [2,1]
- C0456388
- UMLS CUI [2,2]
- C0344211
Description
Blood product; Blood product, Supportive care
Type de données
text
Alias
- UMLS CUI [1]
- C0456388
- UMLS CUI [2,1]
- C0456388
- UMLS CUI [2,2]
- C0344211
Description
Blood product, Cumulative Dose; Blood product, Supportive care, Cumulative Dose
Type de données
text
Alias
- UMLS CUI [1,1]
- C0456388
- UMLS CUI [1,2]
- C2986497
- UMLS CUI [2,1]
- C0456388
- UMLS CUI [2,2]
- C0344211
- UMLS CUI [2,3]
- C2986497
Description
Blood product, Unit of Measure; Blood product, Supportive care, Unit of Measure
Type de données
text
Alias
- UMLS CUI [1,1]
- C0456388
- UMLS CUI [1,2]
- C1519795
- UMLS CUI [2,1]
- C0456388
- UMLS CUI [2,2]
- C0344211
- UMLS CUI [2,3]
- C1519795
Description
Blood product, Start Date; Blood product, Supportive care, Start Date
Type de données
date
Alias
- UMLS CUI [1,1]
- C0456388
- UMLS CUI [1,2]
- C0808070
- UMLS CUI [2,1]
- C0456388
- UMLS CUI [2,2]
- C0344211
- UMLS CUI [2,3]
- C0808070
Description
Blood product, End Date; Blood product, Supportive care, End Date
Type de données
date
Alias
- UMLS CUI [1,1]
- C0456388
- UMLS CUI [1,2]
- C0806020
- UMLS CUI [2,1]
- C0456388
- UMLS CUI [2,2]
- C0344211
- UMLS CUI [2,3]
- C0806020
Description
Pharmacogenetic (PGx) Research Consent / Whole Blood Sample Collection
Alias
- UMLS CUI-1
- C0005834
- UMLS CUI-2
- C2347500
- UMLS CUI-3
- C0021430
Description
Pharmacogenetic Test, Informed Consent
Type de données
boolean
Alias
- UMLS CUI [1,1]
- C2347500
- UMLS CUI [1,2]
- C0021430
Description
Pharmacogenetic Test, Informed Consent, Date in time
Type de données
date
Alias
- UMLS CUI [1,1]
- C2347500
- UMLS CUI [1,2]
- C0021430
- UMLS CUI [1,3]
- C0011008
Description
Pharmacogenetic Test, Collection of blood specimen for laboratory procedure
Type de données
boolean
Alias
- UMLS CUI [1,1]
- C2347500
- UMLS CUI [1,2]
- C0005834
Description
Pharmacogenetic Test, Collection of blood specimen for laboratory procedure, Date in time
Type de données
date
Alias
- UMLS CUI [1,1]
- C2347500
- UMLS CUI [1,2]
- C0005834
- UMLS CUI [1,3]
- C0011008
Description
Pharmacogenetic Test, Informed Consent, Reason and justification
Type de données
text
Alias
- UMLS CUI [1,1]
- C2347500
- UMLS CUI [1,2]
- C0021430
- UMLS CUI [1,3]
- C0566251
Description
Pharmacogenetic Test, Informed Consent, Reason and justification
Type de données
text
Alias
- UMLS CUI [1,1]
- C2347500
- UMLS CUI [1,2]
- C0021430
- UMLS CUI [1,3]
- C0566251
Description
Pharmacogenetic (PGx) Research Withdrawal of Consent
Alias
- UMLS CUI-1
- C2347500
- UMLS CUI-2
- C0021430
- UMLS CUI-3
- C2349954
Description
Pharmacogenetic Test, Informed Consent, Withdraw (activity)
Type de données
boolean
Alias
- UMLS CUI [1,1]
- C2347500
- UMLS CUI [1,2]
- C0021430
- UMLS CUI [1,3]
- C2349954
Description
Pharmacogenetic Test, Informed Consent, Withdraw (activity), Date in time
Type de données
date
Alias
- UMLS CUI [1,1]
- C2347500
- UMLS CUI [1,2]
- C0021430
- UMLS CUI [1,3]
- C2349954
- UMLS CUI [1,4]
- C0011008
Description
Pharmacogenetic Test, Blood specimen, Destruction (action), Request - action
Type de données
boolean
Alias
- UMLS CUI [1,1]
- C2347500
- UMLS CUI [1,2]
- C0178913
- UMLS CUI [1,3]
- C1948029
- UMLS CUI [1,4]
- C1272683
Description
Pharmacogenetic Test, Blood specimen, Destruction (action), Request - action, Reason and justification
Type de données
text
Alias
- UMLS CUI [1,1]
- C2347500
- UMLS CUI [1,2]
- C0178913
- UMLS CUI [1,3]
- C1948029
- UMLS CUI [1,4]
- C1272683
- UMLS CUI [1,5]
- C0566251
Description
Pharmacogenetic Test, Blood specimen, Destruction (action), Request - action, Reason and justification
Type de données
text
Alias
- UMLS CUI [1,1]
- C2347500
- UMLS CUI [1,2]
- C0178913
- UMLS CUI [1,3]
- C1948029
- UMLS CUI [1,4]
- C1272683
- UMLS CUI [1,5]
- C0566251
Similar models
Log
- StudyEvent: ODM
C2985720 (UMLS CUI-2)
C2985720 (UMLS CUI [2])
C0001617 (UMLS CUI [1,2])
C0456388 (UMLS CUI [2,1])
C0344211 (UMLS CUI [2,2])
C0031325 (UMLS CUI [1,2])
C2348184 (UMLS CUI [1,2])
C2826798 (UMLS CUI [1,2])
C1140263 (UMLS CUI [1,2])
C3898442 (UMLS CUI [1,2])
C0805701 (UMLS CUI [1,2])
C0231175 (UMLS CUI [1,3])
C0808070 (UMLS CUI [1,2])
C1705586 (UMLS CUI [1,2])
C0806020 (UMLS CUI [1,2])
C0439603 (UMLS CUI [1,2])
C0518690 (UMLS CUI [1,2])
C0806909 (UMLS CUI [1,3])
C0441800 (UMLS CUI [1,2])
C0806909 (UMLS CUI [1,3])
C0441800 (UMLS CUI [1,2])
C0806909 (UMLS CUI [1,3])
C1518404 (UMLS CUI [2,1])
C0518690 (UMLS CUI [2,2])
C0806909 (UMLS CUI [2,3])
C1704758 (UMLS CUI [1,2])
C2349954 (UMLS CUI [1,2])
C0439849 (UMLS CUI [1,2])
C0304229 (UMLS CUI [1,3])
C2926735 (UMLS CUI [1,2])
C0449244 (UMLS CUI [1,2])
C0946444 (UMLS CUI [1,3])
C0332307 (UMLS CUI [1,2])
C0304229 (UMLS CUI [1,2])
C2348184 (UMLS CUI [1,2])
C2826798 (UMLS CUI [1,2])
C1140263 (UMLS CUI [1,2])
C3898442 (UMLS CUI [1,2])
C0805701 (UMLS CUI [1,2])
C0231175 (UMLS CUI [1,3])
C0808070 (UMLS CUI [1,2])
C1705586 (UMLS CUI [1,2])
C0806020 (UMLS CUI [1,2])
C1519255 (UMLS CUI [2,1])
C1148348 (UMLS CUI [2,2])
C0518690 (UMLS CUI [1,2])
C0806909 (UMLS CUI [1,3])
C0441800 (UMLS CUI [1,2])
C0806909 (UMLS CUI [1,3])
C0441800 (UMLS CUI [1,2])
C0806909 (UMLS CUI [1,3])
C1519255 (UMLS CUI [2,1])
C0518690 (UMLS CUI [2,2])
C0806909 (UMLS CUI [2,3])
C1704758 (UMLS CUI [1,2])
C2349954 (UMLS CUI [1,2])
C0439849 (UMLS CUI [1,2])
C0304229 (UMLS CUI [1,3])
C2926735 (UMLS CUI [1,2])
C0449244 (UMLS CUI [1,2])
C0946444 (UMLS CUI [1,3])
C0439849 (UMLS CUI [1,2])
C2348568 (UMLS CUI [1,3])
C1710056 (UMLS CUI [1,2])
C2347852 (UMLS CUI [1,2])
C2348184 (UMLS CUI [1,3])
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])
C1519795 (UMLS CUI [1,3])
C2347852 (UMLS CUI [1,2])
C0439603 (UMLS CUI [1,3])
C2347852 (UMLS CUI [1,2])
C0013153 (UMLS CUI [1,3])
C2347852 (UMLS CUI [1,2])
C0808070 (UMLS CUI [1,3])
C2826666 (UMLS CUI [1,2])
C2347852 (UMLS CUI [1,2])
C0806020 (UMLS CUI [1,3])
C0012634 (UMLS CUI [1,2])
C0035648 (UMLS CUI [1,3])
C2348184 (UMLS CUI [1,4])
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])
C0012634 (UMLS CUI [1,2])
C0035648 (UMLS CUI [1,3])
C0205394 (UMLS CUI [1,4])
C0430022 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C2348184 (UMLS CUI [1,4])
C0430022 (UMLS CUI [1,2])
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])
C0205394 (UMLS CUI [1,4])
C0439849 (UMLS CUI [1,2])
C0304229 (UMLS CUI [1,3])
C0947611 (UMLS CUI [1,2])
C2348184 (UMLS CUI [1,2])
C2360065 (UMLS CUI [1,2])
C0871468 (UMLS CUI [1,2])
C0805701 (UMLS CUI [1,2])
C0805701 (UMLS CUI [1,2])
C0231175 (UMLS CUI [1,3])
C0566251 (UMLS CUI [1,2])
C0808070 (UMLS CUI [1,2])
C0806020 (UMLS CUI [1,2])
C0001617 (UMLS CUI-2)
C0001617 (UMLS CUI [1,2])
C2348184 (UMLS CUI [1,3])
C0001617 (UMLS CUI [1,2])
C2360065 (UMLS CUI [1,3])
C0001617 (UMLS CUI [1,2])
C0001617 (UMLS CUI [1,2])
C0871468 (UMLS CUI [1,3])
C0001617 (UMLS CUI [1,2])
C0805701 (UMLS CUI [1,3])
C0001617 (UMLS CUI [1,2])
C0805701 (UMLS CUI [1,3])
C0231175 (UMLS CUI [1,4])
C0001617 (UMLS CUI [1,2])
C2348070 (UMLS CUI [1,3])
C0439810 (UMLS CUI [1,4])
C0001617 (UMLS CUI [1,2])
C1519795 (UMLS CUI [1,3])
C0001617 (UMLS CUI [1,2])
C0439603 (UMLS CUI [1,3])
C0001617 (UMLS CUI [1,2])
C0013153 (UMLS CUI [1,3])
C0001617 (UMLS CUI [1,2])
C0566251 (UMLS CUI [1,3])
C0001617 (UMLS CUI [1,2])
C0566251 (UMLS CUI [1,3])
C0001617 (UMLS CUI [1,2])
C0808070 (UMLS CUI [1,3])
C0001617 (UMLS CUI [1,2])
C0001617 (UMLS CUI [1,2])
C0001617 (UMLS CUI [1,2])
C0806020 (UMLS CUI [1,3])
C0344211 (UMLS CUI-2)
C2348184 (UMLS CUI [1,2])
C0456388 (UMLS CUI [2,1])
C0344211 (UMLS CUI [2,2])
C2348184 (UMLS CUI [2,3])
C0456388 (UMLS CUI [2,1])
C0344211 (UMLS CUI [2,2])
C0456388 (UMLS CUI [2,1])
C0344211 (UMLS CUI [2,2])
C2986497 (UMLS CUI [1,2])
C0456388 (UMLS CUI [2,1])
C0344211 (UMLS CUI [2,2])
C2986497 (UMLS CUI [2,3])
C1519795 (UMLS CUI [1,2])
C0456388 (UMLS CUI [2,1])
C0344211 (UMLS CUI [2,2])
C1519795 (UMLS CUI [2,3])
C0808070 (UMLS CUI [1,2])
C0456388 (UMLS CUI [2,1])
C0344211 (UMLS CUI [2,2])
C0808070 (UMLS CUI [2,3])
C0806020 (UMLS CUI [1,2])
C0456388 (UMLS CUI [2,1])
C0344211 (UMLS CUI [2,2])
C0806020 (UMLS CUI [2,3])
C2347500 (UMLS CUI-2)
C0021430 (UMLS CUI-3)
C0021430 (UMLS CUI [1,2])
C0021430 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,3])
C0005834 (UMLS CUI [1,2])
C0005834 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,3])
C0021430 (UMLS CUI [1,2])
C0566251 (UMLS CUI [1,3])
C0021430 (UMLS CUI [1,2])
C0566251 (UMLS CUI [1,3])
C0021430 (UMLS CUI-2)
C2349954 (UMLS CUI-3)
C0021430 (UMLS CUI [1,2])
C2349954 (UMLS CUI [1,3])
C0021430 (UMLS CUI [1,2])
C2349954 (UMLS CUI [1,3])
C0011008 (UMLS CUI [1,4])
C0178913 (UMLS CUI [1,2])
C1948029 (UMLS CUI [1,3])
C1272683 (UMLS CUI [1,4])
C0178913 (UMLS CUI [1,2])
C1948029 (UMLS CUI [1,3])
C1272683 (UMLS CUI [1,4])
C0566251 (UMLS CUI [1,5])
C0178913 (UMLS CUI [1,2])
C1948029 (UMLS CUI [1,3])
C1272683 (UMLS CUI [1,4])
C0566251 (UMLS CUI [1,5])