ID
24555
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)
- 2017-08-06 2017-08-06 -
Rättsinnehavare
GlaxoSmithKline
Uppladdad den
6 augusti 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 Subject Diary NCT00079911
GSK Valaciclovir for the Suppression and Episodic Treatment of Genital HSV Infection in HIV-Infected Persons Subject Diary NCT00079911
Beskrivning
Genital Herpes Recurrences
Beskrivning
Oral/Other Herpes Recurrences
Beskrivning
date of onset
Datatyp
date
Måttenheter
- day month year
Alias
- UMLS CUI [1,1]
- C0574845
- UMLS CUI [1,2]
- C1274323
Beskrivning
location
Datatyp
integer
Alias
- UMLS CUI [1,1]
- C0450429
- UMLS CUI [1,2]
- C0744883
Beskrivning
If Other, specify
Datatyp
text
Alias
- UMLS CUI [1]
- C0449685
Beskrivning
lnvestigational Product
Beskrivning
Record Any Adverse Events / Illnesses
Beskrivning
Medication Record
Beskrivning
medication start date
Datatyp
date
Alias
- UMLS CUI [1,1]
- C1521826
- UMLS CUI [1,2]
- C0808070
Beskrivning
medication end date
Datatyp
date
Alias
- UMLS CUI [1,1]
- C1521826
- UMLS CUI [1,2]
- C0806020
Beskrivning
medication
Datatyp
text
Alias
- UMLS CUI [1]
- C0013227
Similar models
GSK Valaciclovir for the Suppression and Episodic Treatment of Genital HSV Infection in HIV-Infected Persons Subject Diary NCT00079911
C0920316 (UMLS CUI [1,2])
C1115441 (UMLS CUI [1,3])
C1274323 (UMLS CUI [1,2])
C1274323 (UMLS CUI [1,2])
C1709043 (UMLS CUI [1,2])
C0808070 (UMLS CUI [1,2])
C0806020 (UMLS CUI [1,2])