ID
24555
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)
- 06-08-17 06-08-17 -
Houder van rechten
GlaxoSmithKline
Geüploaded op
6 augustus 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 Subject Diary NCT00079911
GSK Valaciclovir for the Suppression and Episodic Treatment of Genital HSV Infection in HIV-Infected Persons Subject Diary NCT00079911
Beschrijving
Genital Herpes Recurrences
Beschrijving
Oral/Other Herpes Recurrences
Beschrijving
date of onset
Datatype
date
Maateenheden
- day month year
Alias
- UMLS CUI [1,1]
- C0574845
- UMLS CUI [1,2]
- C1274323
Beschrijving
location
Datatype
integer
Alias
- UMLS CUI [1,1]
- C0450429
- UMLS CUI [1,2]
- C0744883
Beschrijving
If Other, specify
Datatype
text
Alias
- UMLS CUI [1]
- C0449685
Beschrijving
lnvestigational Product
Beschrijving
Record Any Adverse Events / Illnesses
Beschrijving
Medication Record
Beschrijving
medication start date
Datatype
date
Alias
- UMLS CUI [1,1]
- C1521826
- UMLS CUI [1,2]
- C0808070
Beschrijving
medication end date
Datatype
date
Alias
- UMLS CUI [1,1]
- C1521826
- UMLS CUI [1,2]
- C0806020
Beschrijving
medication
Datatype
text
Alias
- UMLS CUI [1]
- C0013227
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GSK Valaciclovir for the Suppression and Episodic Treatment of Genital HSV Infection in HIV-Infected Persons Subject Diary NCT00079911
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