ID

21398

Beschrijving

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: HLA-B*5701 Results Medicine: abacavir, Condition: Infection, Human Immunodeficiency Virus, Phase: 4, Clinical Study ID: CNA106030, Sponsor: ViiV

Trefwoorden

  1. 19-04-17 19-04-17 -
Geüploaded op

19 april 2017

DOI

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Licentie

Creative Commons BY-NC 3.0

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

Genetic Screening For HLA-B*5701 HLA-B*5701 Results NCT00340080

HLA-B*5701 Results
Beschrijving

HLA-B*5701 Results

Alias
UMLS CUI-1
C0679560
UMLS CUI-2
C1274040
Subject Identifier
Beschrijving

Subject Identifier

Datatype

text

Alias
UMLS CUI [1]
C2348585
Does the subject want the option of receiving his or her HLA-B*5701 results when the results are available ?
Beschrijving

During the informed consent process, the subject is asked if he/she would like the option of receiving his/her HLA- B*5701 results when the results are available. The subject’s response is captured on the informed consent form using yes/no checkboxes. The subject’s response should be transcribed from the informed consent form to the CRF page.

Datatype

text

Alias
UMLS CUI [1,1]
C1514756
UMLS CUI [1,2]
C0679560
UMLS CUI [1,3]
C1274040

Similar models

Genetic Screening For HLA-B*5701 HLA-B*5701 Results NCT00340080

Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
HLA-B*5701 Results
C0679560 (UMLS CUI-1)
C1274040 (UMLS CUI-2)
Subject Identifier
Item
Subject Identifier
text
C2348585 (UMLS CUI [1])
Item
Does the subject want the option of receiving his or her HLA-B*5701 results when the results are available ?
text
C1514756 (UMLS CUI [1,1])
C0679560 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
Code List
Does the subject want the option of receiving his or her HLA-B*5701 results when the results are available ?
CL Item
Yes (Y)
CL Item
No (N)

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