ID
24393
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)
- 2017-07-30 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 NON SERIOUS ADVERSE EVENTS NCT00079911
GSK Valaciclovir for the Suppression and Episodic Treatment of Genital HSV Infection in HIV-Infected Persons NON SERIOUS ADVERSE EVENTS NCT00079911
Beskrivning
NON SERIOUS ADVERSE EVENTS
Beskrivning
NON SERIOUS ADVERSE EVENTS
Beskrivning
Diagnosis Only (if known) Otherwise Sign/Symptom e.g., Headache
Datatyp
text
Alias
- UMLS CUI [1]
- C0877248
Beskrivning
adverse event start date
Datatyp
date
Måttenheter
- DD/MMM/YY
Alias
- UMLS CUI [1]
- C2697888
Beskrivning
Outcome
Datatyp
integer
Alias
- UMLS CUI [1]
- C1705586
Beskrivning
adverse event end date
Datatyp
date
Måttenheter
- DD/MMM/YY
Alias
- UMLS CUI [1]
- C2697886
Beskrivning
Maximum Intensity
Datatyp
text
Alias
- UMLS CUI [1,1]
- C1710056
- UMLS CUI [1,2]
- C1518404
Beskrivning
Action taken with investigational product
Datatyp
text
Alias
- UMLS CUI [1,1]
- C1704758
- UMLS CUI [1,2]
- C1518404
Beskrivning
Withdrawal
Datatyp
text
Alias
- UMLS CUI [1,1]
- C1710677
- UMLS CUI [1,2]
- C1518404
Beskrivning
Relationship to investigational products
Datatyp
text
Alias
- UMLS CUI [1,1]
- C0085978
- UMLS CUI [1,2]
- C0877248
Similar models
GSK Valaciclovir for the Suppression and Episodic Treatment of Genital HSV Infection in HIV-Infected Persons NON SERIOUS ADVERSE EVENTS NCT00079911
C1518404 (UMLS CUI [1,2])
C1518404 (UMLS CUI [1,2])
C0877248 (UMLS CUI [1,2])