ID

32632

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

  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

Follow-Up: Study Conclusion

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

Study Conclusion Data
Descrizione

Study Conclusion Data

Date of subject completion or withdrawal
Descrizione

Date of subject completion or withdrawal

Tipo di dati

date

Time of subject completion or withdrawal
Descrizione

Time of subject completion or withdrawal

Tipo di dati

time

Was the subject withdrawn from the study?
Descrizione

Was the subject withdrawn from the study?

Tipo di dati

boolean

If YES, specify primary reason for withdrawal
Descrizione

If YES, specify primary reason for withdrawal

Tipo di dati

text

If OTHER, specify
Descrizione

If OTHER, specify

Tipo di dati

text

Case book ready for signature
Descrizione

Data owner should check the box when data cleaning is complete

Tipo di dati

text

Office Use 1
Descrizione

Office Use 1

Tipo di dati

boolean

Office Use 2
Descrizione

Office Use 2

Tipo di dati

text

Similar models

Follow-Up: Study Conclusion

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
Study Conclusion Data
Date of subject completion or withdrawal
Item
Date of subject completion or withdrawal
date
Time of subject completion or withdrawal
Item
Time of subject completion or withdrawal
time
Was the subject withdrawn from the study?
Item
Was the subject withdrawn from the study?
boolean
Item
If YES, specify primary reason for withdrawal
text
Code List
If YES, specify primary reason for withdrawal
CL Item
Adverse event (1)
CL Item
Lost to follow-up (2)
CL Item
Protocol violation (3)
CL Item
Subject decided to withdraw from the study (4)
CL Item
Sponsor terminated study (5)
CL Item
Other (6)
If OTHER, specify
Item
If OTHER, specify
text
Item
Case book ready for signature
text
Code List
Case book ready for signature
CL Item
Yes (1)
Office Use 1
Item
Office Use 1
boolean
Item
Office Use 2
text
Code List
Office Use 2
CL Item
1 (1)
CL Item
2 (2)
CL Item
3 (3)
CL Item
4 (4)
CL Item
5 (5)
CL Item
6 (6)
CL Item
7 (7)
CL Item
8 (8)
CL Item
9 (9)

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