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To evaluate the effect of ranitidine on immunologic indicators in asymptomatic HIV-1 infected patients with CD4 counts of 400-700 cells/mm3.
Patients are randomized to receive either ranitidine or matching placebo bid for 16 weeks, with follow-up every 4 weeks through week 20.
Age
18 - No limit years
Sex
ALL
Healthy Volunteers
No
Pacific Oaks Med Group
Sherman Oaks, California, United States
Community Research Initiative
Coral Gables, Florida, United States
Duke Univ Med Ctr
Durham, North Carolina, United States
Houston Clinical Research Network
Houston, Texas, United States
Last Updated
June 24, 2005
104
Estimated participants
Ranitidine hydrochloride
DRUG
Lead Sponsor
Glaxo Wellcome
NCT04142047
NCT06694805
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.
View ClinicalTrials.gov Terms and ConditionsNCT07428330