ID

23717

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 (1)
  1. 7/11/17 7/11/17 -
Copyright Holder

GlaxoSmithKline

Uploaded on

July 11, 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 Screening Visit CENTRAL LABORATORY- BLOOD NCT00079911

English

GSK Study Screening Visit CENTRAL LABORATORY- BLOOD NCT00079911

1 forms  
Study administration
Description

Study administration

Subject Identifier
Description

Subject Identifier

Data type

integer

Alias
UMLS CUI [1]
C2348585
Visit Date
Description

Visit Date

Data type

date

Measurement units
  • DD/MMM/YY
Alias
UMLS CUI [1]
C1320303
DD/MMM/YY
CENTRAL LABORATORY - BLOOD
Description

CENTRAL LABORATORY - BLOOD

Date sample taken
Description

Date sample taken

Data type

date

Measurement units
  • DD/MMM/YY
Alias
UMLS CUI [1]
C1302413
DD/MMM/YY
PREGNANCY TEST PROMPT
Description

Record the results of the blood pregnancy test on the Pregnancy Test running log pages.

Data type

text

HIV RNA PROMPT
Description

Ensure that a blood sample is obtained for HIV viral load analysis.

Data type

text

SEROLOGY PROMPT
Description

Ensure that blood samples are obtained for HSV serology analysis.

Data type

text

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Similar models

GSK Study Screening Visit CENTRAL LABORATORY- BLOOD 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])
Visit Date
Item
Visit Date
date
C1320303 (UMLS CUI [1])
Item Group
CENTRAL LABORATORY - BLOOD
Date sample taken
Item
Date sample taken
date
C1302413 (UMLS CUI [1])
PREGNANCY TEST PROMPT
Item
PREGNANCY TEST PROMPT
text
HIV RNA PROMPT
Item
HIV RNA PROMPT
text
SEROLOGY PROMPT
Item
SEROLOGY PROMPT
text
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