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

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  1. 25/04/17 25/04/17 -
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25 aprile 2017

DOI

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Creative Commons BY-NC 3.0
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Genetic Screening For HLA-B*5701 in Patients with HIV Study Conclusion NCT00340080

Anglais

Genetic Screening For HLA-B*5701 Study Conclusion NCT00340080

1 Formulaires  
Study Conclusion
Description

Study Conclusion

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

Subject Identifier

Type de données

text

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

Date of subject completion or withdrawal

Type de données

date

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Was the subject withdrawn from the study?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

subject withdrawn

Type de données

text

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

Reason for withdrawal

Type de données

integer

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

Reason for withdrawal

Type de données

text

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

Genetic Screening For HLA-B*5701 Study Conclusion NCT00340080

1 Formulaires
Name
Type
Description | Question | Decode (Coded Value)
Type de données
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Was the subject withdrawn from the study?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])
subject withdrawn
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Was the subject withdrawn from the study?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])
Reason for withdrawal
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])
Retour au début de la page 

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