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| Sponsored by: |
LyphoMed |
| Information provided by: | NIH AIDS Clinical Trials Information Service |
| ClinicalTrials.gov Identifier: | NCT00002292 |
Purpose
To compare parenteral versus inhaled pentamidine in patients with documented Pneumocystis carinii pneumonia (PCP) with AIDS.
| Condition | Intervention |
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Pneumonia, Pneumocystis Carinii HIV Infections |
Drug: Pentamidine isethionate |
| MedlinePlus related topics: | AIDS Pneumonia |
| Drug Information available for: | Pentamidine |
| Study Type: | Interventional |
| Study Design: | Treatment, Randomized |
| Official Title: | Inhaled Versus Intravenous Pentamidine in Pneumocystis Carinii Pneumonia in the Acquired Immunodeficiency Syndrome |
Eligibility
| Ages Eligible for Study: | 18 Years and older |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Exclusion Criteria
Co-existing Condition:
Patients with the following are excluded:
Patients with the following are excluded:
All patients hospitalized at Cedars-Sinai Medical Center with AIDS and possible Pneumocystis carinii pneumonia (PCP) will be eligible.
Contacts and Locations
More Information
| Study ID Numbers: | 023B, 88-001 |
| First Received: | November 2, 1999 |
| Last Updated: | June 23, 2005 |
| ClinicalTrials.gov Identifier: | NCT00002292 |
| Health Authority: | United States: Food and Drug Administration |
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