ID

24388

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

Versions (2)
  1. 7/30/17 7/30/17 -
  2. 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 HIV ASSOCIATED CONDITIONS NCT00079911

English

GSK Valaciclovir for the Suppression and Episodic Treatment of Genital HSV Infection in HIV-Infected Persons HIV ASSOCIATED CONDITIONS NCT00079911

1 forms  
Study administration
Description

Study administration

Subject Identifier
Description

Subject Identifier

Data type

integer

Alias
UMLS CUI [1]
C2348585
HIV-ASSOCIATED CONDITIONS
Description

HIV-ASSOCIATED CONDITIONS

Did the subject experience any HIV-associated conditions on or after Randomization Visit?
Description

If Yes, record HIV-associated conditions experienced on or after Randomization Visit below using the codes on facing page.

Data type

text

Alias
UMLS CUI [1]
C0276555
HIV-ASSOCIATED CONDITIONS
Description

HIV-ASSOCIATED CONDITIONS

HIV-Associated Conditions If code 'BOT' (Other), provide text
Description

HIV-Associated Conditions

Data type

text

Alias
UMLS CUI [1]
C0276555
Start Date
Description

Start Date

Data type

date

Measurement units
  • DD/MMM/YY
Alias
UMLS CUI [1,1]
C0808070
UMLS CUI [1,2]
C0276555
DD/MMM/YY
Has the subject previously had this condition?
Description

previously had this condition

Data type

text

Alias
UMLS CUI [1]
C0276555
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Similar models

GSK Valaciclovir for the Suppression and Episodic Treatment of Genital HSV Infection in HIV-Infected Persons HIV ASSOCIATED CONDITIONS NCT00079911

1 forms
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
HIV-ASSOCIATED CONDITIONS
Item
Did the subject experience any HIV-associated conditions on or after Randomization Visit?
text
C0276555 (UMLS CUI [1])
HIV-associated conditions
Code List
Did the subject experience any HIV-associated conditions on or after Randomization Visit?
CL Item
Yes (Y)
CL Item
No (N)
Item Group
HIV-ASSOCIATED CONDITIONS
HIV-Associated Conditions
Item
HIV-Associated Conditions If code 'BOT' (Other), provide text
text
C0276555 (UMLS CUI [1])
Start Date
Item
Start Date
date
C0808070 (UMLS CUI [1,1])
C0276555 (UMLS CUI [1,2])
Item
Has the subject previously had this condition?
text
C0276555 (UMLS CUI [1])
previously had this condition
Code List
Has the subject previously had this condition?
CL Item
No (N)
CL Item
Yes (Y)
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