ID

32704

Beschrijving

Study ID: 107038 Clinical Study ID: LPL107038 Study Title: Study to Estimate the Dose Proportionality of the Enteric-Coated Freebase Formulation of SB-480848 Patient Level Data:  Clinicaltrials.gov Identifier:  Sponsor: GlaxoSmithKline Collaborators: N/A Phase: Phase 1 Study Recruitment Status: Completed Generic Name: darapladib Trade Name: Tyrisa ,US Study Indication: Atherosclerosis

Trefwoorden

  1. 13-11-18 13-11-18 -
Houder van rechten

GSK group of companies

Geüploaded op

13 november 2018

DOI

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Licentie

Creative Commons BY-NC 3.0

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Estimation of Dose Proportionality of Darapladib - 107038

Follow-Up: Study Conclusion

Study Conclusion Data
Beschrijving

Study Conclusion Data

Date of subject completion or withdrawal
Beschrijving

Date of subject completion or withdrawal

Datatype

date

Time of subject completion or withdrawal
Beschrijving

Time of subject completion or withdrawal

Datatype

time

Was the subject withdrawn from the study?
Beschrijving

Was the subject withdrawn from the study?

Datatype

boolean

If YES, specify primary reason for withdrawal
Beschrijving

If YES, specify primary reason for withdrawal

Datatype

text

If OTHER, specify
Beschrijving

If OTHER, specify

Datatype

text

Case book ready for signature
Beschrijving

Data owner should check the box when data cleaning is complete

Datatype

text

Office Use 1
Beschrijving

Office Use 1

Datatype

boolean

Office Use 2
Beschrijving

Office Use 2

Datatype

text

Similar models

Follow-Up: Study Conclusion

Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
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Was the subject withdrawn from the study?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Was the subject withdrawn from the study?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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