NCT Number: NCT00385645
Atazanavir or Lopinavir in HIV Post-exposure Prophylaxis
The study compares the adherence of 240 HIV-negative subjects randomly assigned to 2 different antiretroviral therapies for 28 days after accidental exposure to HIV.
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Notify MeKey information
Conditions
Age range
18 year and older
Sex eligibility
All sexes
Study type
Interventional
Phase
Phase 4
Primary location
Hospital Universitari Germans Trias i Pujol, Badalona, Barcelona, Spain
Who can participate
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
- Age > 18
- HIV exposure requiring prophylaxis under current guidelines
Exclusion criteria
- Pregnancy
- Suspected drug resistance in source case
- Contraindications to the study drugs
Treatment and study plan
Combivir+Reyataz
DrugPrimary outcomes
-
Proportions of patients completing 28-day antiretroviral treatment (ARVT)
Secondary outcomes
-
Proportion of HIV-seropositive at 6 months
-
Incidence of adverse effects (clinical and laboratory) during ARVT
-
Adherence to ARVT, time to adherence loss.
Sponsors and collaborators
Lead sponsor
Hospital Clinic of Barcelona
Other
Registry information
Official study title
Comparison of 2 Alternative Antiretroviral Combinations in HIV Post-exposure Prophylaxis: AZT-3TC (Combivir®) + Lopinavir-ritonavir (Kaletra®) Versus AZT-3TC (Combivir®)+ Atazanavir (Reyataz®). Multicentre, Prospective, Randomized, Open Study
Important dates
- Study start
- 2006
- Primary completion
- 2009
- Study completion
- 2009
- First posted
- Oct 11, 2006
- Registry last updated
- Mar 31, 2010
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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