ID

32635

Descrizione

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

Keywords

versioni (2)
  1. 09/11/18 09/11/18 -
  2. 11/01/19 11/01/19 -
Titolare del copyright

GSK group of companies

Caricato su

9 novembre 2018

DOI

Per favore, per richiedere un accesso.

Licenza

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

Inglese

Logs and Repeats: Adverse Event and Concomitant Medication Questions

1 moduli  
Administrative data
Descrizione

Administrative data

Site
Descrizione

Site

Tipo di dati

text

Patient
Descrizione

Patient

Tipo di dati

text

Patient Number
Descrizione

Patient Number

Tipo di dati

integer

Date of Visit/Assessment
Descrizione

Date of Visit/Assessment

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

Date below is the start of the study for this subject

Tipo di dati

date

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

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

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

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

Tipo di dati

boolean

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

Did the subject experience any adverse events during the study?

Tipo di dati

boolean

Were any repeat ECGs performed?
Descrizione

Were any repeat ECGs performed?

Tipo di dati

boolean

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

Did the subject have any abnormal ECGs during the study?

Tipo di dati

boolean

Were any repeat vital signs recorded?
Descrizione

Were any repeat vital signs recorded?

Tipo di dati

boolean

Were any repeat PK taken?
Descrizione

Were any repeat PK taken?

Tipo di dati

boolean

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Similar models

Logs and Repeats: Adverse Event and Concomitant Medication Questions

1 moduli
Name
genere
Description | Question | Decode (Coded Value)
Tipo di dati
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
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