ID

21397

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: Expanded PGx-Pharmacogenetic Research Medicine: abacavir, Condition: Infection, Human Immunodeficiency Virus, Phase: 4, Clinical Study ID: CNA106030, Sponsor: ViiV

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Versions (1)
  1. 19/04/2017 19/04/2017 -
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19 avril 2017

DOI

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Licence

Creative Commons BY-NC 3.0
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Genetic Screening For HLA-B*5701 in Patients with HIV Expanded PGx-Pharmacogenetic Research NCT00340080

Anglais

Genetic Screening For HLA-B*5701 Expanded PGx-Pharmacogenetic Research NCT00340080

1 Formulaires  
Expanded PGx-Pharmacogenetic Research
Description

Expanded PGx-Pharmacogenetic Research

Alias
UMLS CUI-1
C2347500
UMLS CUI-2
C0008976
Subject Identifier
Description

Subject Identifier

Type de données

text

Alias
UMLS CUI [1]
C2348585
Has informed consent been obtained for expanded PGx-Pharmacogenetic research on safety/tolerability of HAART?
Description

informed consent

Type de données

text

Alias
UMLS CUI [1]
C0021430
If Yes, record the date informed consent obtained for Expanded PGx-Pharmacogenetic research on safety/tolerability of HAART
Description

date informed consent obtained

Type de données

date

Alias
UMLS CUI [1,1]
C0514044
UMLS CUI [1,2]
C0011008
If No, check 􏰀one reason:
Description

reason informed consent not obtained

Type de données

integer

Alias
UMLS CUI [1,1]
C0392360
UMLS CUI [1,2]
C0021430
UMLS CUI [1,3]
C1882120
If other reason please specify
Description

reason informed consent not obtained

Type de données

text

Alias
UMLS CUI [1,1]
C0392360
UMLS CUI [1,2]
C0021430
UMLS CUI [1,3]
C1882120
Has subject withdrawn consent for expanded PGx-Pharmacogenetic research on safety/tolerability of HAART?
Description

Withdrawal of consent

Type de données

text

Alias
UMLS CUI [1]
C1707492
Retour au début de la page

Similar models

Genetic Screening For HLA-B*5701 Expanded PGx-Pharmacogenetic Research NCT00340080

1 Formulaires
Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Item Group
Expanded PGx-Pharmacogenetic Research
C2347500 (UMLS CUI-1)
C0008976 (UMLS CUI-2)
Subject Identifier
Item
Subject Identifier
text
C2348585 (UMLS CUI [1])
Item
Has informed consent been obtained for expanded PGx-Pharmacogenetic research on safety/tolerability of HAART?
text
C0021430 (UMLS CUI [1])
informed consent
Code List
Has informed consent been obtained for expanded PGx-Pharmacogenetic research on safety/tolerability of HAART?
CL Item
Yes (Y)
CL Item
No (N)
date informed consent obtained
Item
If Yes, record the date informed consent obtained for Expanded PGx-Pharmacogenetic research on safety/tolerability of HAART
date
C0514044 (UMLS CUI [1,1])
C0011008 (UMLS CUI [1,2])
Item
If No, check 􏰀one reason:
integer
C0392360 (UMLS CUI [1,1])
C0021430 (UMLS CUI [1,2])
C1882120 (UMLS CUI [1,3])
reason informed consent not obtained
Code List
If No, check 􏰀one reason:
CL Item
Subject declined (1)
CL Item
Subject not asked by Investigator (2)
CL Item
Other (3)
reason informed consent not obtained
Item
If other reason please specify
text
C0392360 (UMLS CUI [1,1])
C0021430 (UMLS CUI [1,2])
C1882120 (UMLS CUI [1,3])
Item
Has subject withdrawn consent for expanded PGx-Pharmacogenetic research on safety/tolerability of HAART?
text
C1707492 (UMLS CUI [1])
informed consent
Code List
Has subject withdrawn consent for expanded PGx-Pharmacogenetic research on safety/tolerability of HAART?
CL Item
Yes (Y)
CL Item
No (N)
Retour au début de la page 

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