ID

21516

Description

NCT00340080 / VIIV-CNA106030 A phase IV, randomised, multicentre, double-blind, study to evaluate the clinical utility of prospective genetic screening (HLA-B*5701) for susceptibility to abacavir hypersensitivity Assessment: Study Conclusion Medicine: abacavir, Condition: Infection, Human Immunodeficiency Virus, Phase: 4, Clinical Study ID: CNA106030, Sponsor: ViiV

Keywords

  1. 4/25/17 4/25/17 -
Uploaded on

April 25, 2017

DOI

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License

Creative Commons BY-NC 3.0

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Genetic Screening For HLA-B*5701 in Patients with HIV Study Conclusion NCT00340080

Genetic Screening For HLA-B*5701 Study Conclusion NCT00340080

Study Conclusion
Description

Study Conclusion

Alias
UMLS CUI-1
C1707478
UMLS CUI-2
C0008976
Subject Identifier
Description

Subject Identifier

Data type

text

Alias
UMLS CUI [1]
C2348585
Date of subject completion or withdrawal
Description

Date of subject completion or withdrawal

Data type

date

Alias
UMLS CUI [1]
C2983670
Was the subject withdrawn from the study?
Description

subject withdrawn

Data type

text

Alias
UMLS CUI [1]
C0422727
If yes, select the primary reason for withdrawal
Description

Reason for withdrawal

Data type

integer

Alias
UMLS CUI [1,1]
C2349954
UMLS CUI [1,2]
C0392360
Reason for withdrawal: Other, specify
Description

Reason for withdrawal

Data type

text

Alias
UMLS CUI [1,1]
C2349954
UMLS CUI [1,2]
C0392360

Similar models

Genetic Screening For HLA-B*5701 Study Conclusion NCT00340080

Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
Study Conclusion
C1707478 (UMLS CUI-1)
C0008976 (UMLS CUI-2)
Subject Identifier
Item
Subject Identifier
text
C2348585 (UMLS CUI [1])
Date of subject completion or withdrawal
Item
Date of subject completion or withdrawal
date
C2983670 (UMLS CUI [1])
Item
Was the subject withdrawn from the study?
text
C0422727 (UMLS CUI [1])
Code List
Was the subject withdrawn from the study?
CL Item
Yes (Y)
CL Item
No (N)
Item
If yes, select the primary reason for withdrawal
integer
C2349954 (UMLS CUI [1,1])
C0392360 (UMLS CUI [1,2])
Code List
If yes, select the 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 (6)
CL Item
Non-compliance (17)
CL Item
Did not meet treatment eligibility criteria (24)
CL Item
Investigator Decision (26)
CL Item
Other (7)
Reason for withdrawal
Item
Reason for withdrawal: Other, specify
text
C2349954 (UMLS CUI [1,1])
C0392360 (UMLS CUI [1,2])

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