Single-Blind Efficacy Evaluation of Intravenous Spiramycin in Subjects With AIDS-Related Cryptosporidial Diarrhea
Spiramycin
Infections transmises par le sang+30
+ Maladies génito-urinaires
+ Maladies Génitales
Étude thérapeutique
Résumé
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.
Protocole
Cette section fournit des détails sur le plan de l'étude, y compris la manière dont l'étude est conçue et ce qu'elle évalue.25 participants à inclure
Nombre total de participants que l'essai clinique vise à recruter.Traitement
Éligibilité
Les chercheurs recherchent des patients correspondant à une certaine description appelée critères d'éligibilité : état de santé général ou traitements antérieurs du patient.Tout sexe
Le sexe biologique des participants éligibles à s'inscrire.À partir de 13 ans
Tranche d'âge des participants éligibles à participer.Volontaires sains non autorisés
Indique si les individus en bonne santé et ne présentant pas la condition étudiée peuvent participer.Conditions
Pathologie
Critères
Inclusion Criteria Concurrent Medication: Allowed: Vitamin supplements. Zidovudine (AZT) for patients previously taking AZT. However, dosing with spiramycin should be delayed until the dose of AZT has stabilized. The dose may be decreased for AZT-associated toxicity. Allowed for diarrhea: Loperamide hydrochloride capsules (2 mg) or loperamide hydrochloride liquid (1 mg/5 ml). Allowed for nausea: Sucralfate and metoclopramide hydrochloride. Allowed for vomiting: Prochlorperazine and trimethobenzamide hydrochloride. Allowed as prophylaxis for Pneumocystis carinii pneumonia (PCP): Aerosolized pentamidine. Patients must have: A diagnosis of AIDS according to the CDC. Chronic diarrhea. Presence of Cryptosporidium oocysts in stool specimen. Patients or a legally authorized representative must sign an informed consent form. Diet will be lactose free, maximum 7 g fat/day with unlimited calorie intake. Patients who require total parenteral nutrition will also be allowed oral intake. Exclusion Criteria Co-existing Condition: Patients with the following are excluded: Grade 4 (for hematologic) or Grade 3 (for all other) toxicity. Known sensitivity to macrolide antibiotics. Presence of other diarrhea-causing pathogens. Active opportunistic infection requiring systemic antimicrobial therapy. Toxicity grades according to NIAID toxicity scale for adults. Concurrent Medication: Excluded: Other investigational drugs. Cancer chemotherapy. Alpha interferon. Other immunomodulating agents. Other macrolide antibiotics. Trimethoprim / sulfamethoxazole. Ganciclovir. H2 blockers and AL-721. Medications known to cause gastrointestinal irritation or alteration of gastrointestinal motility or absorption should be avoided if possible. Zidovudine (AZT) therapy may not be initiated and the dose may not be increased during the study. Patients with the following are excluded: Grade 4 (for hematologic) or Grade 3 (for all other) toxicity. Known sensitivity to macrolide antibiotics. Presence of other diarrhea-causing pathogens. Active opportunistic infection requiring systemic antimicrobial therapy. Toxicity grades according to NIAID toxicity scale for adults. Prior Medication: Excluded within 7 days of study entry: Investigational drugs. Excluded within 14 days of study entry: Cancer chemotherapy. Alpha interferon. Other immunomodulating agents. Other macrolide antibiotics. Trimethoprim / sulfamethoxazole. Ganciclovir.
Centres d'étude
Ce sont les hôpitaux, cliniques ou centres de recherche où l'essai est conduit. Vous pouvez trouver le site le plus proche de vous ainsi que son statut.Cette étude comporte 7 sites
Johns Hopkins Univ School of Medicine
Baltimore, United StatesUniv of Massachusetts Med Ctr
Worcester, United StatesBellevue Hosp / New York Univ Med Ctr
New York, United States