ID
42299
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)
- 5/12/21 5/12/21 -
Copyright Holder
GlaxoSmithKline
Uploaded on
May 12, 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)
Pharmacogenetics
- StudyEvent: ODM
Description
Date of visit/assessment
Alias
- UMLS CUI-1
- C1320303
- UMLS CUI-3
- C2985720
Description
PGx-Pharmacogenetic Research Consent
Alias
- UMLS CUI-1
- C2347500
- UMLS CUI-3
- C0021430
Description
Has informed consent been otained for PGx-Pharmacogenetic research?
Data type
boolean
Alias
- UMLS CUI [1]
- C0021430
- UMLS CUI [2]
- C2347500
Description
Date informed consent obtained for PGx-Pharmacogenetic research
Data type
date
Alias
- UMLS CUI [1]
- C0021430
- UMLS CUI [2]
- C2347500
- UMLS CUI [3]
- C0011008
Description
Has a blood sample been collected for PGx-Pharmacogenetic (DNA) research?
Data type
boolean
Alias
- UMLS CUI [1,1]
- C2347500
- UMLS CUI [1,2]
- C0005834
Description
Record Date sample taken
Data type
date
Alias
- UMLS CUI [1]
- C1302413
Description
If no informed consent has been obtained for PGx-Pharmacogenetic research, check reason
Data type
integer
Alias
- UMLS CUI [1]
- C0021430
- UMLS CUI [2]
- C2347500
- UMLS CUI [3]
- C0392360
Description
If other reason for informed consent has not been obtained, specify
Data type
text
Alias
- UMLS CUI [1]
- C0021430
- UMLS CUI [2,1]
- C0566251
- UMLS CUI [2,2]
- C0205394
- UMLS CUI [2,3]
- C2348235
Description
Genetics Type
Data type
text
Alias
- UMLS CUI [1,1]
- C0017399
- UMLS CUI [1,2]
- C0332307
Description
Pharmacogenetic Research Withdrawal of Consent
Alias
- UMLS CUI-1
- C1707492
- UMLS CUI-3
- C0031325
Description
Has subject withdrawn consent for PGx-Pharmacogenetic research?
Data type
boolean
Alias
- UMLS CUI [1]
- C2347500
- UMLS CUI [2,1]
- C0021430
- UMLS CUI [2,2]
- C2349954
Description
Has a request been made for sample destruction?
Data type
boolean
Alias
- UMLS CUI [1]
- C1948029
- UMLS CUI [2]
- C0178913
- UMLS CUI [3]
- C1272683
Description
If request for sample destruction has been made, check reason
Data type
integer
Alias
- UMLS CUI [1]
- C1948029
- UMLS CUI [2]
- C0178913
- UMLS CUI [3]
- C1272683
- UMLS CUI [4]
- C0392360
Description
Specify other reason for sample destruction
Data type
text
Alias
- UMLS CUI [1]
- C1948029
- UMLS CUI [2]
- C0178913
- UMLS CUI [3]
- C0392360
- UMLS CUI [4,1]
- C0205394
- UMLS CUI [4,2]
- C2348235
Description
Genetics Type
Data type
text
Alias
- UMLS CUI [1,1]
- C0017399
- UMLS CUI [1,2]
- C0332307
Similar models
Pharmacogenetics
- StudyEvent: ODM
C2985720 (UMLS CUI-3)
C2985720 (UMLS CUI [1,2])
C0021430 (UMLS CUI-3)
C2347500 (UMLS CUI [2])
C2347500 (UMLS CUI [2])
C0011008 (UMLS CUI [3])
C0005834 (UMLS CUI [1,2])
C2347500 (UMLS CUI [2])
C0392360 (UMLS CUI [3])
C0566251 (UMLS CUI [2,1])
C0205394 (UMLS CUI [2,2])
C2348235 (UMLS CUI [2,3])
C0332307 (UMLS CUI [1,2])
C0031325 (UMLS CUI-3)
C0021430 (UMLS CUI [2,1])
C2349954 (UMLS CUI [2,2])
C0178913 (UMLS CUI [2])
C1272683 (UMLS CUI [3])
C0178913 (UMLS CUI [2])
C1272683 (UMLS CUI [3])
C0392360 (UMLS CUI [4])
C0178913 (UMLS CUI [2])
C0392360 (UMLS CUI [3])
C0205394 (UMLS CUI [4,1])
C2348235 (UMLS CUI [4,2])
C0332307 (UMLS CUI [1,2])