An interventional study of Indinavir sulfate and Ritonavir in HIV Infections, sponsored by Abbott. Completed at 6 sites in United States. Open to participants aged 12 Years and older. Per ClinicalTrials.gov, last updated 2009-02-20.
Sponsored by Abbott · Not applicable, Interventional, and Treatment
The purpose of this study is to determine how many HIV-infected patients continue taking ritonavir/indinavir combination after having taken indinavir three times a day as part of their anti-HIV drug therapy. This study also examines the safety and effectiveness of the ritonavir/indinavir combination.
4,258 studies on the registry are indexed under HIV Infections; 240 are open to participants now.
Browse HIV Infections studies →Abbott is the lead sponsor of 350 studies on the registry; 1 is open to participants now.
Counted across the registry records on this site, refreshed daily.
Patients must have:
Exclusion Criteria
Co-existing Condition:
Patients with any of the following symptoms or conditions are excluded:
Any condition that in the opinion of the investigator may obscure proper observation of the safety or activity of the treatment regimens used in this study.
Concurrent Medication:
Excluded:
Patients with the following prior conditions are excluded:
Prior Medication:
Excluded:
Prior treatment with ritonavir.
Risk Behavior:
Excluded:
History of active substance abuse (i.e., recreational drugs or alcohol).
Included:
This study is completed, as verified in Feb 2009. You cannot join it, but the record below documents what was studied.
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