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A Study of Spiramycin in the Treatment of Patients With AIDS-Related Diarrhea

Phase 1
Completed
Conditions
Cryptosporidiosis
HIV Infections
Registration Number
NCT00000980
Lead Sponsor
Rhone-Poulenc Rorer
Brief Summary

To determine the safety and effectiveness of intravenous spiramycin in patients with AIDS-related cryptosporidial diarrhea.

Spiramycin, a macrolide antibiotic, has been studied in the United States for the treatment of cryptosporidial diarrhea. Some reports suggest that spiramycin is useful in improving the symptoms of cryptosporidial diarrhea in some patients. Results of one study, however, showed no significant difference between spiramycin and placebo (inactive medication). A later study indicated that the absorption of spiramycin is significantly decreased when food is present. Thus, the results of the trial may have been due to poor absorption of spiramycin.

Detailed Description

Spiramycin, a macrolide antibiotic, has been studied in the United States for the treatment of cryptosporidial diarrhea. Some reports suggest that spiramycin is useful in improving the symptoms of cryptosporidial diarrhea in some patients. Results of one study, however, showed no significant difference between spiramycin and placebo (inactive medication). A later study indicated that the absorption of spiramycin is significantly decreased when food is present. Thus, the results of the trial may have been due to poor absorption of spiramycin.

Patients are observed for 3 days to establish baseline conditions. They are informed that the treatment period is 21 days during which they receive 15 days of spiramycin and 6 consecutive days of placebo; they are not told which 6-day period they receive placebo. All patients receive 15 days of spiramycin. Patients who do not have a favorable response are treated with a higher dose of spiramycin for an additional 15 days. Responders at either dose are followed weekly for 4 weeks. Should a relapse occur, patients receive an additional 15 days of therapy, at the dose of spiramycin that initially produced a response, following reestablishment of a baseline with 6 days of placebo. Nonresponders to the higher dose are taken off the study.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
25
Inclusion Criteria

Not provided

Exclusion Criteria

Not provided

Study & Design

Study Type
INTERVENTIONAL
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (7)

Univ Hosp of Cleveland / Case Western Reserve Univ

🇺🇸

Cleveland, Ohio, United States

Nelson Tebedo Community Clinic

🇺🇸

Dallas, Texas, United States

Kaiser Permanente Med Ctr

🇺🇸

San Diego, California, United States

Johns Hopkins Univ School of Medicine

🇺🇸

Baltimore, Maryland, United States

Bellevue Hosp / New York Univ Med Ctr

🇺🇸

New York, New York, United States

Univ of Massachusetts Med Ctr

🇺🇸

Worcester, Massachusetts, United States

Cornell Univ Med Ctr

🇺🇸

New York, New York, United States

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