ID

24375

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. 2017-07-30 2017-07-30 -
Rättsinnehavare

GlaxoSmithKline

Uppladdad den

30 juli 2017

DOI

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Licens

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 INVESTIGATIONAL PRODUCT NCT00079911

Engelsk

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

1 Formulär  
Study administration
Beskrivning

Study administration

Subject Identifier
Beskrivning

Subject Identifier

Datatyp

integer

Alias
UMLS CUI [1]
C2348585
INVESTIGATIONAL PRODUCT
Beskrivning

INVESTIGATIONAL PRODUCT

Investigational Product
Beskrivning

Check carefully for any overlapping start/stop date. Ensure any deviations from investigational product are recorded correctly as outlined in the study protocol. Record a new start and stop date if greater than or equal to one day of dosing is missed.

Datatyp

integer

Alias
UMLS CUI [1]
C0304229
Start date
Beskrivning

pharmacotherapy start date

Datatyp

date

Måttenheter
  • DD/MMM/YY
Alias
UMLS CUI [1,1]
C0013216
UMLS CUI [1,2]
C0808070
DD/MMM/YY
Stop date
Beskrivning

pharmacotherapy stop date

Datatyp

date

Måttenheter
  • DD/MMM/YY
Alias
UMLS CUI [1,1]
C0013216
UMLS CUI [1,2]
C0806020
DD/MMM/YY
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Similar models

GSK Valaciclovir for the Suppression and Episodic Treatment of Genital HSV Infection in HIV-Infected Persons INVESTIGATIONAL PRODUCT 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])
Item Group
INVESTIGATIONAL PRODUCT
Item
Investigational Product
integer
C0304229 (UMLS CUI [1])
Investigational Product
Code List
Investigational Product
CL Item
Double-Blind therapy (23)
CL Item
Open-label treatment (24)
pharmacotherapy start date
Item
Start date
date
C0013216 (UMLS CUI [1,1])
C0808070 (UMLS CUI [1,2])
pharmacotherapy stop date
Item
Stop date
date
C0013216 (UMLS CUI [1,1])
C0806020 (UMLS CUI [1,2])
Tillbaka till toppen 

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