A Randomized Open-Label Study of the Tolerability and Efficacy of Clarithromycin and Ethambutol in Combination With or Without Clofazimine for the Treatment of Disseminated MAC (dMAC) in Patients With AIDS
Ethambutol hydrochloride
+ Clarithromycin
+ Clofazimine
Infecciones Transmitidas por la Sangre+12
+ Enfermedades Urogenitales
+ Enfermedades Genitales
Estudio de Tratamiento
Resumen
Fecha de inicio: 1 de enero de 1994
Fecha en la que se inscribió al primer participante.PRIMARY: To assess the tolerability of the combination regimen of clarithromycin plus ethambutol with or without clofazimine in patients with disseminated Mycobacterium avium Complex (dMAC). SECONDARY: To determine the proportion of patients achieving a sterile blood culture along with the time required to achieve it. To determine the duration of bacteriological response, defined as length of time that blood cultures remain sterile.
Protocolo
Esta sección proporciona detalles del plan del estudio, incluyendo cómo está diseñado y qué se está evaluando.Estudio de Tratamiento
Elegibilidad
Los investigadores buscan pacientes que cumplan ciertos criterios, conocidos como criterios de elegibilidad: estado general de salud o tratamientos previos.Cualquier sexo
Sexo biológico de los participantes elegibles para inscribirse.A partir de 13 años
Rango de edades de los participantes que pueden unirse al estudio.Voluntarios sanos no permitidos
Indica si personas sanas, sin la condición que se estudia, pueden participar.Condiciones
Patología
Criterios
Inclusion Criteria Patients must have: History of HIV seropositivity. Disseminated MAC. Positive blood culture for MAC within 4 weeks prior to study entry. Consent of parent or guardian if less than 18 years of age. Ability to complete the study. NOTE: Patients with active opportunistic infections other than dMAC are permitted if dosage and clinical parameters have been stable for 4 weeks prior to enrollment. Exclusion Criteria Concurrent Medication: Excluded: Active therapy with carbamazepine or theophylline, unless investigator agrees to carefully monitor blood levels. Active therapy with investigational drugs other than treatment for HIV disease, except with approval of the sponsor. Concomitant terfenadine (Seldane or Seldane-D) or astemizole (Hismanal). Amikacin. Azithromycin. Capreomycin. Ciprofloxacin. Cycloserine. Ethionamide. Gentamicin. Kanamycin. Levofloxacin. Lomefloxacin. Ofloxacin. Rifampin. Rifabutin. Sparfloxacin. Streptomycin. Any other aminoglycosides, quinolones, and macrolides. Patients with the following prior conditions are excluded: History of allergy or hypersensitivity to macrolides, ethambutol, or clofazimine. Prior Medication: Excluded: Other antimycobacterials, including aminoglycosides, ansamycin (rifabutin), other macrolides (such as clindamycin), quinolones, and rifampin, between screening and study entry. Clarithromycin or azithromycin as prophylaxis or treatment (for any cause) for more than 14 days cumulative within the past 2 months.
Centros del Estudio
Estos son los hospitales, clínicas o centros de investigación donde se lleva a cabo el estudio. Puedes encontrar la ubicación más cercana a ti y su estado de reclutamiento.Este estudio tiene 18 ubicaciones
UCD Med Ctr
Sacramento, United StatesKaiser Permanente Med Ctr
San Francisco, United StatesSanta Clara Valley Med Ctr
San Jose, United States