Status:
COMPLETED
Aerosols in the Treatment of Pneumocystis Pneumonia: A Pilot Study Quantitating the Deposition of Aerosolized Pentamidine as Delivered in ACTG 040 and Comparing Its Toxicity With Parenteral Pentamidine Therapy
Lead Sponsor:
National Institute of Allergy and Infectious Diseases (NIAID)
Conditions:
Pneumonia, Pneumocystis Carinii
HIV Infections
Eligibility:
All Genders
12+ years
Phase:
NA
Brief Summary
To compare the use of pentamidine aerosol (inhaled mist) with the standard intravenous method of administration in patients with AIDS related Pneumocystis carinii pneumonia (PCP), to measure the amoun...
Detailed Description
Aerosolized pentamidine was as effective as intravenous pentamidine in treating PCP in animals. More of the pentamidine reached the lungs and less was found in the liver and kidney after pentamidine w...
Eligibility Criteria
Inclusion Criteria
Prior Medication:
Allowed:
- Prophylaxis for Pneumocystis carinii pneumonia (PCP); zidovudine.
Unequivocal diagnosis of Pneumocystis carinii pneumonia (PCP) established by morphological confirmation of three or more typical Pneumocystis carinii organisms in bronchoalveolar lavage fluid, obtained immediately following the initial inhalation of radiolabeled aerosol.
- Resting (A-a) DO2 < 30 torr on room air or resting (A-a) DO2 = or < 55 torr on room air with a serious intolerance to trimethoprim / sulfamethoxazole (TMP / SMX), defined as one or more of the following:
- Platelets < 50000 platelets/mm3 or absolute neutrophil count (polys plus bands) = or < 500 cells/mm3 on at least two occasions = or > 12 hours apart.
- Blistering rash, mucosal involvement, generalized maculopapular eruption, or intolerable pruritus.
- Transaminase > 5 x ULN or = or > 300 IU if baseline is abnormal.
- Daily temperature = or > 103 degrees F beginning after the 5th day of treatment and persisting for at least 3 days and not responsive to antipyretic therapy, with no other discernible cause.
- Any other severe or life-threatening adverse reaction to TMP / SMX that, in the investigator's opinion, makes continued or recurrent treatment with TMP / SMX inadvisable (approved on a case-by-case basis by the NIAID clinical monitor).
Exclusion Criteria
Co-existing Condition:
Patients with the following conditions or diseases are excluded:
- Dyspnea, cough, bronchospasm, or other reasons causing inability to cooperate with aerosol administration.
- History of major adverse reaction to pentamidine.
Patients with the following conditions or diseases are excluded:
- Dyspnea, cough, bronchospasm, or other reasons causing inability to cooperate with aerosol administration.
- History of major adverse reaction to pentamidine.
Prior Medication:
Excluded:
- Other antiprotozoal regimens.
- Excluded within 14 days of entry:
- Systemic steroids > adrenal replacement doses
Key Trial Info
Start Date :
Trial Type :
INTERVENTIONAL
End Date :
June 1 1991
Estimated Enrollment :
45 Patients enrolled
Trial Details
Trial ID
NCT00000722
End Date
June 1 1991
Last Update
November 3 2021
Active Locations (1)
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1
SUNY - Stony Brook
Stony Brook, New York, United States, 117948153