ID

32635

Descrição

Study ID: 106904 Clinical Study ID: CRV106904 Study Title: A Randomized, Open-Label, Single-Dose, Four-Period Cross-Over Study to Determine the Effects of Alcohol on the Pharmacokinetics of Carvedilol CR Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier:  Sponsor: GlaxoSmithKline Collaborators: N/A Phase: Phase 1 Study Recruitment Status: Completed Generic Name: carvedilol Trade Name: Coreg CR,Coreg Study Indication: Hypertension

Palavras-chave

Versões (2)
  1. 09/11/2018 09/11/2018 -
  2. 11/01/2019 11/01/2019 -
Titular dos direitos

GSK group of companies

Transferido a

9 de novembro de 2018

DOI

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Licença

Creative Commons BY-NC 3.0
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A Cross-Over Study of Alcohol Effect on the Pharmacokinetics of Carvedilol - 106904

Inglês

Logs and Repeats: Adverse Event and Concomitant Medication Questions

1 Formulários  
Administrative data
Descrição

Administrative data

Site
Descrição

Site

Tipo de dados

text

Patient
Descrição

Patient

Tipo de dados

text

Patient Number
Descrição

Patient Number

Tipo de dados

integer

Date of Visit/Assessment
Descrição

Date of Visit/Assessment

Date below is the start of the study for this subject
Descrição

Date below is the start of the study for this subject

Tipo de dados

date

Adverse Event/Concomitant Medications/Repeat Assessment (Check Questions)
Descrição

Adverse Event/Concomitant Medications/Repeat Assessment (Check Questions)

Were any concomitant medications taken by the subject during the study?
Descrição

Were any concomitant medications taken by the subject during the study?

Tipo de dados

boolean

Did the subject experience any adverse events during the study?
Descrição

Did the subject experience any adverse events during the study?

Tipo de dados

boolean

Were any repeat ECGs performed?
Descrição

Were any repeat ECGs performed?

Tipo de dados

boolean

Did the subject have any abnormal ECGs during the study?
Descrição

Did the subject have any abnormal ECGs during the study?

Tipo de dados

boolean

Were any repeat vital signs recorded?
Descrição

Were any repeat vital signs recorded?

Tipo de dados

boolean

Were any repeat PK taken?
Descrição

Were any repeat PK taken?

Tipo de dados

boolean

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Similar models

Logs and Repeats: Adverse Event and Concomitant Medication Questions

1 Formulários
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de dados
Alias
Item Group
Administrative data
Site
Item
Site
text
Patient
Item
Patient
text
Patient Number
Item
Patient Number
integer
Item Group
Date of Visit/Assessment
Date below is the start of the study for this subject
Item
Date below is the start of the study for this subject
date
Item Group
Adverse Event/Concomitant Medications/Repeat Assessment (Check Questions)
Were any concomitant medications taken by the subject during the study?
Item
Were any concomitant medications taken by the subject during the study?
boolean
Did the subject experience any adverse events during the study?
Item
Did the subject experience any adverse events during the study?
boolean
Were any repeat ECGs performed?
Item
Were any repeat ECGs performed?
boolean
Did the subject have any abnormal ECGs during the study?
Item
Did the subject have any abnormal ECGs during the study?
boolean
Were any repeat vital signs recorded?
Item
Were any repeat vital signs recorded?
boolean
Were any repeat PK taken?
Item
Were any repeat PK taken?
boolean
Voltar ao início da página 

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