ID

24377

Description

NCT00079911 Study ID 100181 Clinical Study ID HS2100181 Study Title: An International, Randomized, Double-Blind, Placebo-Controlled Study of Valaciclovir for the Suppression and Episodic Treatment of Genital HSV Infection in HIV-Infected Persons with CD4+ lymphocyte count <100 cells/mm3. Patient Level Data Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: NCT00079911 Sponsor: GlaxoSmithKline Collaborators: N/A Phase: Phase 4 Study Recruitment Status: Terminated Generic Name: valaciclovir Trade Name: ZELITREX,Valtrex,RAPIVIR,Novirus Study Indication: Genital Herpes; HIV infection

Keywords

  1. 7/30/17 7/30/17 -
Copyright Holder

GlaxoSmithKline

Uploaded on

July 30, 2017

DOI

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License

Creative Commons BY-NC 3.0

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GSK Valaciclovir for the Suppression and Episodic Treatment of Genital HSV Infection in HIV-Infected Persons STATUS OF TREATMENT BLIND NCT00079911

GSK Valaciclovir for the Suppression and Episodic Treatment of Genital HSV Infection in HIV-Infected Persons STATUS OF TREATMENT BLIND NCT00079911

Study administration
Description

Study administration

Subject Identifier
Description

Subject Identifier

Data type

integer

Alias
UMLS CUI [1]
C2348585
STATUS OF TREATMENT BLIND
Description

STATUS OF TREATMENT BLIND

Was the treatment blind broken during the study?
Description

blind broken

Data type

text

Alias
UMLS CUI [1,1]
C0034656
UMLS CUI [1,2]
C3897431
Date blind broken
Description

If Yes, complete the following

Data type

date

Alias
UMLS CUI [1,1]
C0034656
UMLS CUI [1,2]
C3897431
UMLS CUI [1,3]
C0011008
Reason blind broken
Description

Reason blind broken

Data type

text

Alias
UMLS CUI [1,1]
C0392360
UMLS CUI [1,2]
C0034656
UMLS CUI [1,3]
C3897431
Other, specify
Description

specify reason

Data type

text

Alias
UMLS CUI [1,1]
C0392360
UMLS CUI [1,2]
C0034656
UMLS CUI [1,3]
C3897431

Similar models

GSK Valaciclovir for the Suppression and Episodic Treatment of Genital HSV Infection in HIV-Infected Persons STATUS OF TREATMENT BLIND NCT00079911

Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
Study administration
Subject Identifier
Item
Subject Identifier
integer
C2348585 (UMLS CUI [1])
Item Group
STATUS OF TREATMENT BLIND
Item
Was the treatment blind broken during the study?
text
C0034656 (UMLS CUI [1,1])
C3897431 (UMLS CUI [1,2])
Code List
Was the treatment blind broken during the study?
CL Item
Yes (Y)
CL Item
No (N)
date blind broken
Item
Date blind broken
date
C0034656 (UMLS CUI [1,1])
C3897431 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,3])
Item
Reason blind broken
text
C0392360 (UMLS CUI [1,1])
C0034656 (UMLS CUI [1,2])
C3897431 (UMLS CUI [1,3])
Code List
Reason blind broken
CL Item
Medical emergency requiring identification of investigational product for further treatment (1)
CL Item
Other, specify (Z)
specify reason
Item
Other, specify
text
C0392360 (UMLS CUI [1,1])
C0034656 (UMLS CUI [1,2])
C3897431 (UMLS CUI [1,3])

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