A Multi-Center Clinical Trial To Evaluate Azidothymidine (AZT) in the Treatment of Human Immunodeficiency Virus (HIV) Infection in Patients With AIDS Post First Episode PCP
Collecte de données
Infections transmises par le sang+24
+ Maladies génito-urinaires
+ Maladies Génitales
Étude thérapeutique
Résumé
Previous studies have shown the effectiveness of AZT in AIDS therapy. AZT has been effective in test tube studies at varying doses. There is a need to see if lower doses result in effective therapy with less harmful side effects. Patients are assigned at random to one of two treatment programs: (1) 1 dose of AZT given orally (PO) for 6 doses per day; (2) 2 doses of AZT PO for 4 weeks followed by 1 dose PO for the remainder of the trial.
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.482 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 12 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: * All concomitant medication to minimum and record. * Any approved medications can be used to treat an opportunistic infection. * Dapsone may be used for Pneumocystis carinii pneumonia (PCP). * Pyrimethamine - sulfadoxine may be used for toxoplasmosis. * Ganciclovir for cytomegalovirus may be used for maintenance only. * Prophylactic therapy for PCP. Concurrent Treatment: Allowed: * Local, limited radiation therapy to isolated Kaposi's sarcoma lesions provided total area is \< 5 x 5 cm and a 6-MeV electron beam or 90 kV x-ray = or \< 3000 rads total is used. Patients must have: * HIV seropositivity as confirmed by any federally licensed ELISA test kit. * Allowed: * Malignancy in past which has been in complete remission for 1 year without therapy. Exclusion Criteria Co-existing Condition: Patients with active opportunistic infections will be excluded. Concurrent Medication: Excluded: * Aspirin on a regular basis or beyond 72 hours without contacting investigator. * Cimetidine. * Flurazepam. * Indomethacin. * Ranitidine. * Probenecid. Patients with the following are excluded: * Status post-Pneumocystis carinii pneumonia with symptomatic visceral Kaposi's sarcoma (KS) or progression of KS within the month prior to study entry. * Other concurrent neoplasms other than basal cell carcinoma of the skin. * Requiring blood transfusions \> once per month. Last transfusion cannot have been given within 7 days of entry. * Active substance abuse. Unwilling to sign informed consent or to be followed at medical center where enrolled for duration of study and follow-up if necessary. Prior Medication: Excluded within 2 weeks of study entry: * Treatment for acute Pneumocystis carinii pneumonia (PCP). * Excluded within 30 days of study entry: * Other antiretroviral agents, immunomodulating agents, or corticosteroids. Prior Treatment: Excluded within 30 days of study entry: * Radiation therapy or cytotoxic chemotherapy for Kaposi's sarcoma. Required: * Patients must be at least 2 weeks post- therapy status for acute Pneumocystis carinii pneumonia (PCP).
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 28 sites
Los Angeles County - USC Med Ctr
Los Angeles, United StatesOuvrir Los Angeles County - USC Med Ctr dans Google MapsUCLA CARE Ctr
Los Angeles, United StatesUniv of California / San Diego Treatment Ctr
San Diego, United StatesSan Francisco AIDS Clinic / San Francisco Gen Hosp
San Francisco, United States