ID
42296
Description
Study ID: 105533 Clinical Study ID: 105533 Study Title: A randomized, open-label, single-dose, four period cross-over study to evaluate the relative bioavailability of four formulations of GSK lisinopril compared to Zestril, and to compare over-incapsulated Zestril to Zestril Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Sponsor: GlaxoSmithKline Phase: Phase 1 Study Recruitment Status: Completed Generic Name: Carvedilol Trade Name: Zestril Study Indication: Hypertension
Keywords
Versions (1)
- 5/10/21 5/10/21 -
Copyright Holder
GlaxoSmithKline
Uploaded on
May 10, 2021
DOI
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License
Creative Commons BY 4.0
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Relative bioavailability of four formulations of GSK lisinopril compared to Zestril (105533)
Follow-Up: Study Conclusion; Pregnancy Information
- StudyEvent: ODM
Description
Date of visit/assessment
Alias
- UMLS CUI-1
- C1320303
- UMLS CUI-2
- C2985720
Description
Study Conclusion
Alias
- UMLS CUI-1
- C1707478
- UMLS CUI-2
- C0008972
Description
Date/time of subject completion or withdrawal
Data type
datetime
Alias
- UMLS CUI [1,1]
- C0008976
- UMLS CUI [1,2]
- C1707478
- UMLS CUI [2]
- C1264639
Description
Was the subject withdrawn from the study?
Data type
boolean
Alias
- UMLS CUI [1]
- C0422727
Description
Primary Reason for withdrawal
Data type
integer
Alias
- UMLS CUI [1,1]
- C0422727
- UMLS CUI [1,2]
- C0392360
Description
Specify other reason for withdrawal
Data type
text
Alias
- UMLS CUI [1,1]
- C0422727
- UMLS CUI [1,2]
- C0392360
- UMLS CUI [2]
- C0205394
- UMLS CUI [3]
- C2348235
Description
Data owner should check the box when data cleaning is complete
Data type
text
Alias
- UMLS CUI [1]
- C1519316
Description
Pregnancy Information
Alias
- UMLS CUI-1
- C0032961
- UMLS CUI-2
- C1533716
Similar models
Follow-Up: Study Conclusion; Pregnancy Information
- StudyEvent: ODM
C2985720 (UMLS CUI-2)
C2985720 (UMLS CUI [1,2])
C1707478 (UMLS CUI [1,2])
C1264639 (UMLS CUI [2])
C0392360 (UMLS CUI [1,2])
C0392360 (UMLS CUI [1,2])
C0205394 (UMLS CUI [2])
C2348235 (UMLS CUI [3])