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A Double-Blind Placebo-Controlled Group Comparative Study To Evaluate the Safety and Effectiveness of Aerosol Pentamidine in the Prophylaxis of Pneumocystis Carinii Pneumonia in Patients With AIDS Post First Episode PCP

A Double-Blind Placebo-Controlled Group Comparative Study To Evaluate the Safety and Effectiveness of Aerosol Pentamidine in the Prophylaxis of Pneumocystis Carinii Pneumonia in Patients With AIDS Post First Episode PCP

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00002053
Enrollment
Unknown
Registered
2001-08-31
Start date
Unknown
Completion date
Unknown
Last updated
2005-06-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

HIV Infections, Pneumonia, Pneumocystis Carinii

Keywords

AIDS-Related Opportunistic Infections, Pneumonia, Pneumocystis carinii, Pentamidine, Acquired Immunodeficiency Syndrome

Brief summary

To evaluate and compare the safety, tolerability, and efficacy of biweekly administration of aerosol pentamidine versus placebo when used as a prophylactic agent in patients who have recovered from their first episode of AIDS-associated Pneumocystis carinii pneumonia (PCP).

Interventions

DRUGPentamidine isethionate

Sponsors

Fisons
Lead SponsorINDUSTRY

Study design

Primary purpose
TREATMENT
Masking
DOUBLE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

Concurrent Medication: Allowed: * Zidovudine (AZT). If AZT is started during the study, patients must have received = or \> 15 days of aerosol pentamidine before beginning AZT. Prior Medication: Allowed: * Zidovudine (AZT). If AZT began prior to study entry, patients must have received = or \> 15 days of AZT before beginning aerosol pentamidine.

Exclusion criteria

Co-existing Condition: Patients with the following are excluded: * Requiring ongoing active therapy for an opportunistic infection (O.I.) at time of entry or those with either of the following AIDS-defining O.I.'s prior to entry: * Toxoplasmosis. * Cryptococcosis. * Transfusion dependent (requiring blood transfusion more than once per month). The last transfusion cannot have been given within 7 days of study entry. * Pulmonary Kaposi's sarcoma (KS). * Uncontrolled asthma. * Active therapy for tuberculosis. Patients with the following are excluded: * Requiring ongoing active therapy for an opportunistic infection (O.I.) at time of entry or those with either of the following AIDS-defining O.I.'s prior to entry: * Toxoplasmosis. * Cryptococcosis. * Transfusion dependent (requiring blood transfusion more than once per month). The last transfusion cannot have been given within 7 days of study entry. * Pulmonary Kaposi's sarcoma (KS). * Uncontrolled asthma. Prior Medication: Excluded within 30 days of study entry: * Antiretroviral agents other than zidovudine (AZT). * Immunomodulating agents. * Corticosteroids. Active therapy for tuberculosis. Patients must: * Have AIDS and recovered from their first episode of Pneumocystis carinii pneumonia (PCP). * Be at least 2 weeks and no more than 24 weeks status post therapy for acute PCP. * Have positive antibody to HIV by a Government-approved ELISA test kit, or confirmed Western blot test. * Adequate pulmonary function (vital capacity = or \> 80 percent of predicted; forced expiratory volume (FEV), 1 s = or \> 65 percent of total FEV; and corrected pulmonary diffusion capacity \> 60 percent of predicted). * Free of acute medical problems. Active substance abuse.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026