ID

32614

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

  1. 08/11/2018 08/11/2018 -
  2. 13/12/2018 13/12/2018 -
  3. 13/12/2018 13/12/2018 -
Titular dos direitos

GSK group of companies

Transferido a

8 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

Session 3: Treatment Confirmation

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

Treatment Confirmation
Descrição

Treatment Confirmation

Did the subject receive the correct treatment (e.g., treatment which the subject was assigned to) during this dosing interval?
Descrição

Did the subject receive the correct treatment (e.g., treatment which the subject was assigned to) during this dosing interval?

Tipo de dados

boolean

If NO, record reason(s)
Descrição

If NO, record reason(s)

Tipo de dados

text

Similar models

Session 3: Treatment Confirmation

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
Treatment Confirmation
Did the subject receive the correct treatment (e.g., treatment which the subject was assigned to) during this dosing interval?
Item
Did the subject receive the correct treatment (e.g., treatment which the subject was assigned to) during this dosing interval?
boolean
If NO, record reason(s)
Item
text

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