ID

23720

Beskrivning

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

Nyckelord

Versioner (1)
  1. 2017-07-12 2017-07-12 -
Rättsinnehavare

GlaxoSmithKline

Uppladdad den

12 juli 2017

DOI

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Licens

Creative Commons BY-NC-ND 3.0
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GSK Valaciclovir for the Suppression and Episodic Treatment of Genital HSV Infection in HIV-Infected Persons Randomisation Visit CENTRAL LABORATORY BLOOD NCT00079911

Engelsk

GSK Study Randomisation Visit CENTRAL LABORATORY BLOOD NCT00079911

1 Formulär  
Study administration
Beskrivning

Study administration

Subject Identifier
Beskrivning

Subject Identifier

Datatyp

integer

Alias
UMLS CUI [1]
C2348585
Visit Date
Beskrivning

Visit Date

Datatyp

date

Måttenheter
  • DD/MMM/YY
Alias
UMLS CUI [1]
C1320303
DD/MMM/YY
CENTRAL LABORATORY BLOOD
Beskrivning

CENTRAL LABORATORY BLOOD

Date sample taken
Beskrivning

Date sample taken

Datatyp

date

Alias
UMLS CUI [1]
C1302413
INVESTIGATIONAL PRODUCT CONTAINER NUMBER
Beskrivning

INVESTIGATIONAL PRODUCT CONTAINER NUMBER

Record the identifying number from the investigational product container dispensed at this visit.
Beskrivning

identifying number

Datatyp

integer

Alias
UMLS CUI [1,1]
C2609208
PREGNANCY TEST PROMPT
Beskrivning

PREGNANCY TEST PROMPT

HIV RNA PROMPT
Beskrivning

HIV RNA PROMPT

HIV-ASSOCIATED CONDITIONS
Beskrivning

HIV-ASSOCIATED CONDITIONS

CONCOMITANT MEDICATIONS
Beskrivning

CONCOMITANT MEDICATIONS

ADVERSE EVENTS
Beskrivning

ADVERSE EVENTS

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Similar models

GSK Study Randomisation Visit CENTRAL LABORATORY BLOOD NCT00079911

1 Formulär
Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
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])
Item Group
INVESTIGATIONAL PRODUCT CONTAINER NUMBER
identifying number
Item
Record the identifying number from the investigational product container dispensed at this visit.
integer
C2609208 (UMLS CUI [1,1])
Item Group
PREGNANCY TEST PROMPT
Item Group
HIV RNA PROMPT
Item Group
HIV-ASSOCIATED CONDITIONS
Item Group
CONCOMITANT MEDICATIONS
Item Group
ADVERSE EVENTS
Tillbaka till toppen 

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