ID
41073
Description
Study ID: 103447 Clinical Study ID: NKV103447 Study Title:A study to evaluate the effect of casoptiant on cardiac conduction as assessed by 12-lead electrocardiogram as compared to placebo and moxifloxacin Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Sponsor: GlaxoSmithKline Phase: Phase 1 Study Recruitment Status: Completed Generic Name: casopitant Trade Name: Rezonic,Zunrisa; Zunrisa,Rezonic Study Indication: Nausea and Vomiting, Chemotherapy-Induced
Keywords
Versions (2)
- 6/19/20 6/19/20 -
- 6/19/20 6/19/20 -
Copyright Holder
GlaxoSmithKline
Uploaded on
June 19, 2020
DOI
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License
Creative Commons BY-NC 4.0
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Effect of casoptiant on cardiac conduction as compared to placebo and moxifloxacin 103447
Concomitant Medication
- StudyEvent: ODM
Description
Concomitant Medications
Alias
- UMLS CUI-1
- C2347852 (Concomitant Agent)
Description
If Yes, record each medication on a separate line using Trade Names where possible. If the medication is related to a Non-Serious Adverse Event or Serious Adverse Event, details should be expressed using the same terminology.
Data type
boolean
Alias
- UMLS CUI [1]
- C2347852 (Concomitant Agent)
Description
Concomitant Medications
Alias
- UMLS CUI-1
- C2347852 (Concomitant Agent)
Description
(Trade Name Preferred)
Data type
text
Alias
- UMLS CUI [1]
- C2360065 (Medication name)
- LOINC
- MTHU027854
Description
(eg.500mg)
Data type
float
Alias
- UMLS CUI [1]
- C0869039 (Unit dose)
- SNOMED
- 408102007
Description
Units
Data type
text
Alias
- UMLS CUI [1]
- C1519795 (Unit of Measure)
- SNOMED
- 767524001
Description
(e.g.BID)
Data type
text
Alias
- UMLS CUI [1]
- C3476109 (Medication frequency)
- LOINC
- LP149758-7
Description
Concomitant Medication Route
Data type
text
Alias
- UMLS CUI [1]
- C2826730 (Concomitant Medication Route of Administration)
Description
Reason for Concomitant Medication
Data type
text
Alias
- UMLS CUI [1]
- C2826696 (Concomitant Medication Use Indication)
Description
Concomitant Medication Start Date
Data type
date
Alias
- UMLS CUI [1]
- C2826734 (Concomitant Medication Start Date)
Description
Concomitant Medication Start Time
Data type
time
Alias
- UMLS CUI [1,1]
- C2347852 (Concomitant Agent)
- UMLS CUI [1,2]
- C1301880 (Start time)
- SNOMED
- 398201009
- LOINC
- LP102339-1
Description
Concomitant medication taken prior to study?
Data type
boolean
Alias
- UMLS CUI [1]
- C2826667 (Concomitant Medication Previous Occurrence)
Description
Concomitant Medication Stop Date
Data type
date
Alias
- UMLS CUI [1]
- C2826744 (Concomitant Medication End Date)
Description
Concomitant Medication Stop Time
Data type
time
Alias
- UMLS CUI [1]
- C2826659 (Concomitant Medication End Time)
Description
Ongoing medication?
Data type
boolean
Alias
- UMLS CUI [1]
- C2826666 (Concomitant Medication Ongoing)
Similar models
Concomitant Medication
- StudyEvent: ODM
C1301880 (UMLS CUI [1,2])
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