ID
24275
Beschrijving
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
Trefwoorden
Versies (1)
- 28-07-17 28-07-17 -
Houder van rechten
GlaxoSmithKline
Geüploaded op
28 juli 2017
DOI
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Licentie
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 Month 6 CLINIC VISIT ASSESSMENT NCT00079911
GSK Valaciclovir for the Suppression and Episodic Treatment of Genital HSV Infection in HIV-Infected Persons Month 6 CLINIC VISIT ASSESSMENT NCT00079911
Beschrijving
Clinic Visit Assessment
Alias
- UMLS CUI-1
- C0220825
- UMLS CUI-2
- C0008952
- UMLS CUI-3
- C0019348
Beschrijving
Visit Date
Datatype
date
Alias
- UMLS CUI [1,1]
- C0011008
- UMLS CUI [1,2]
- C0008952
Beschrijving
If Yes, complete the Genital Herpes Recurrences page
Datatype
text
Alias
- UMLS CUI [1,1]
- C0019342
- UMLS CUI [1,2]
- C0034897
Beschrijving
If Yes, complete the Oral/Other Non-Genital Herpes Recurrences page.
Datatype
text
Alias
- UMLS CUI [1]
- C0341012
- UMLS CUI [2]
- C0019348
Similar models
GSK Valaciclovir for the Suppression and Episodic Treatment of Genital HSV Infection in HIV-Infected Persons Month 6 CLINIC VISIT ASSESSMENT NCT00079911
C0008952 (UMLS CUI-2)
C0019348 (UMLS CUI-3)
C0008952 (UMLS CUI [1,2])
C0034897 (UMLS CUI [1,2])
C0019348 (UMLS CUI [2])