Trial of an Alternative Dosing Regimen of Oral Retrovir in Patients With AIDS or Advanced ARC
- Conditions
- HIV Infections
- Registration Number
- NCT00002020
- Lead Sponsor
- Glaxo Wellcome
- Brief Summary
To evaluate the safety and tolerance, in patients with severe clinical manifestations of HIV infection, of zidovudine (AZT) administered daily for 48 weeks as a low dose every 4 hours or a higher dose every 12 hours.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- Not specified
Not provided
Not provided
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (12)
Rush Presbyterian - Saint Luke's Med Ctr
🇺🇸Chicago, Illinois, United States
Northwestern Univ Med School
🇺🇸Chicago, Illinois, United States
North Jersey Community Research Initiative
🇺🇸Newark, New Jersey, United States
Northshore Hosp / Cornell Univ
🇺🇸Manhasset, New York, United States
Univ TX Galveston Med Branch
🇺🇸Galveston, Texas, United States
Cook County Hosp
🇺🇸Chicago, Illinois, United States
Univ of Pennsylvania / HIV Clinic
🇺🇸Philadelphia, Pennsylvania, United States
Univ of Arizona / Health Science Ctr
🇺🇸Tucson, Arizona, United States
Univ of Missouri at Kansas City School of Medicine
🇺🇸Kansas City, Missouri, United States
Univ of New Mexico Hlth Sciences Ctr / Dept of Med
🇺🇸Albuquerque, New Mexico, United States
San Juan Veterans Administration Med Ctr
🇵🇷San Juan, Puerto Rico
Baylor College of Medicine
🇺🇸Houston, Texas, United States