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CompletedNCT00002223Updated Feb 20, 2009

A Study of Ritonavir/Indinavir Combination in HIV-Infected Patients

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

Phase
Not applicable
Study type
Interventional
Ages
12 Years and older
Sex
All
01

Study summary

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.

02

Conditions studied

  • HIV Infections

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Keywords

  • Drug Therapy, Combination
  • Adolescent Behavior
  • HIV Protease Inhibitors
  • Ritonavir
  • Indinavir
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In context

HIV Infections

4,258 studies on the registry are indexed under HIV Infections; 240 are open to participants now.

Browse HIV Infections studies →

Lead sponsor

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.

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Who can participate

Ages eligible
12 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

Patients must have:

  • HIV infection.
  • CD4 cell count greater than 100 cells/microliter.
  • HIV RNA levels greater than 400 copies/microliter using the Roche Ultrasensitive assay.
  • No acute illness.
  • Consent of parent or guardian if less than legal age.
  • No prior enrollment in this study.
  • All entry criteria for this study met within 15 days prior to enrollment.

Exclusion criteria

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:

  • Concurrent non-nucleoside reverse transcriptase inhibitors as part of the antiretroviral regimen.
  • Any of the following medications with ritonavir:
  • midazolam, clorazepate, diazepam, estazolam, flurazepam, triazolam, zolpidem, quinidine, amiodarone, encainide, flecainide, propafenone, bepridil, terfenadine, astemizole, cisapride, bupropion, clozapine, rifabutin, meperidine, propoxyphene, piroxicam, pimozide, dihydroergotamine, and ergotamine.
  • Any of the following medications with indinavir:
  • terfenadine, astemizole, cisapride, triazolam, midazolam. No requirement for rifampin or ketoconazole.
  • Any concurrent treatment with other protease inhibitors.
  • Other concurrent medication (including over-the-counter medicine or alcohol) without the knowledge and permission of the primary investigator.

Patients with the following prior conditions are excluded:

  • History of significant drug hypersensitivity.
  • Psychiatric illness that precludes compliance with the protocol.
  • Receipt of investigational drug within 30 days prior to administration of study drug.
  • History of acute or chronic pancreatitis.
  • Anticipation of poor patient compliance with protocol.

Prior Medication:

Excluded:

Prior treatment with ritonavir.

Risk Behavior:

Excluded:

History of active substance abuse (i.e., recreational drugs or alcohol).

Included:

  • Indinavir 800 mg three times a day plus unspecified nucleosides for at least 3 months.
05

Study design

Phase
Not applicable
Primary purpose
Treatment

Interventions

  • DrugIndinavir sulfate
  • DrugRitonavir
06

Study locations

6 sites
  • AIDS Healthcare Foundation
    Los Angeles, California 90027, United States
  • Tower Infectious Diseases
    Los Angeles, California 90048, United States
  • Urgent Care Ctr / North Broward Hosp District
    Fort Lauderdale, Florida 33316, United States
  • Goodgame Med Ctr / Central Florida Research Initiati
    Maitland, Florida 32751, United States
  • Mount Sinai Med Ctr
    New York, New York 10029, United States
  • Stephen Hauptman
    Philadelphia, Pennsylvania 19107, United States
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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Feb 20, 2009, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT00002223
Lead sponsor
Abbott
First posted
Aug 31, 2001
Last update
Feb 20, 2009
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

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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