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Multi-center Comparison of Fluconazole (UK-49,858) and Amphotericin B as Treatment for Acute Cryptococcal Meningitis

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Qué se está evaluando

Colección de datos

Quiénes están siendo reclutados

Infecciones del Sistema Nervioso Central+21

+ Enfermedades Transmisibles

+ Criptococosis

A partir de 18 años
Ver todos los criterios de elegibilidad
Cómo está diseñado el estudio

Estudio de Tratamiento

Intervencional
Ver detalles del protocolo

Resumen

Patrocinador PrincipalNational Institute of Allergy and Infectious Diseases (NIAID)
Última actualización: 27 de enero de 2026
Extraido de una base de datos validada por el gobierno.Reclamar como socio

Cryptococcal meningitis is an important cause of disease and death among patients with AIDS. Usually AMB is given either alone or with FLC to patients with this infection, but these treatments are not always effective and both have toxic effects. Animal studies and preliminary studies in humans show that FCZ is active in cryptococcal meningitis and suggest that it may be less toxic than either AMB or FLC. Patients accepted into the study are randomly assigned to FCZ or AMB. Patients assigned to FCZ take FCZ by mouth daily for 10 weeks. Patients assigned to AMB are given intravenous injections of AMB daily for 6-10 weeks. Non-AIDS patients assigned to AMB also take FLC by mouth daily. The use of FLC in patients with AIDS is decided on an individual basis. Patients with AIDS who respond satisfactorily to FCZ receive maintenance therapy to prevent relapse for an additional 12 months. Patients with AIDS who respond to AMB may qualify for another Pfizer Central Research protocol. Patients without AIDS who respond to therapy are observed for 6 months for relapse. During therapy, samples of blood and cerebrospinal fluid (by lumbar puncture) are taken periodically in order to evaluate the effectiveness of the drug treatments and to identify possible toxic effects.

Título OficialMulti-center Comparison of Fluconazole (UK-49,858) and Amphotericin B as Treatment for Acute Cryptococcal Meningitis
NCT00000708
Patrocinador PrincipalNational Institute of Allergy and Infectious Diseases (NIAID)
Última actualización: 27 de enero de 2026
Extraido de una base de datos validada por el gobierno.Reclamar como socio

Protocolo

Esta sección proporciona detalles del plan del estudio, incluyendo cómo está diseñado y qué se está evaluando.
Detalles del Diseño

Se reclutarán 120 pacientes

Número total de participantes que el ensayo clínico espera reclutar.

Estudio de Tratamiento

Estos estudios prueban nuevas formas de tratar una enfermedad, condición o problema de salud. El objetivo es determinar si un nuevo medicamento, terapia o enfoque funciona mejor o tiene menos efectos secundarios que las opciones existentes.

Elegibilidad

Los investigadores buscan pacientes que cumplan ciertos criterios, conocidos como criterios de elegibilidad: estado general de salud o tratamientos previos.
Condiciones
Criterios

Cualquier sexo

Sexo biológico de los participantes elegibles para inscribirse.

A partir de 18 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

Infecciones del Sistema Nervioso CentralEnfermedades TransmisiblesCriptococosisEnfermedades UrogenitalesEnfermedades del Sistema Nervioso CentralSíndrome de Inmunodeficiencia AdquiridaEnfermedades NeuroinflamatoriasInfecciones Transmitidas por la SangreEnfermedades GenitalesInfecciones Bacterianas y MicosisEnfermedades del sistema inmunitarioSíndromes de Deficiencia InmunológicaInfeccionesMeningitisMicosisEnfermedades del sistema nerviosoInfecciones OportunistasInfecciones por RetroviridaeInfecciones por virus de ARNEnfermedades de Transmisión SexualEnfermedades por virus lentoEnfermedades ViralesEnfermedades de transmisión sexual, viralesInfecciones por VIH

Criterios

Inclusion Criteria Concurrent Medication: Allowed: * Immunosuppressant therapy. * Cyclosporin plasma concentrations should be monitored and appropriate dosage adjustments made when used with amphotericin B or fluconazole. * Antiviral therapy. * Prophylaxis for Pneumocystis carinii pneumonia. * Treatment of intercurrent opportunistic infection as long as no investigational agent, or approved agent for an investigational indication, is used. * Antipyretics, hydrocortisone, or meperidine to prevent or ameliorate side effects associated with amphotericin B. Concurrent Treatment: Allowed: \- Radiation therapy for mucocutaneous Kaposi's sarcoma. Patients must have: * Written informed consent obtained from the patient or from the patient's legal guardian. * One of the following: * (1) Tentative identification of Cryptococcus neoformans in culture of lumbar cerebrospinal fluid (CSF). Results of baseline cultures need not be available when therapy is begun, but therapy is discontinued if the baseline CSF culture is later found to be negative for C. neoformans, or (2) Clinical and CSF findings (cell count, protein, glucose) compatible with cryptococcal meningitis plus one of the following: * (a) Positive CSF India ink examination, (b) Culture or biopsy evidence of extraneural cryptococcal infection, (c) Positive serum of CSF cryptococcal antigen test, or increase in titer for previously treated patients with suspected relapse, or (d) Biopsy evidence of central nervous system cryptococcal infection. * Treatment status of either no prior systemic antifungal therapy for cryptococcosis or relapse after prior therapy. The success of prior therapy must have been documented by negative CSF culture at the end of therapy. Prior Medication: Allowed within 4 weeks of study entry: \- Successful prior therapy for cryptococcosis, but no more than 1 mg/kg/week amphotericin B. Allowed: * Immunosuppressant therapy. * Antiviral therapy. * Prophylaxis for Pneumocystis carinii pneumonia. Exclusion Criteria Co-existing Condition: Excluded: * Acute or chronic meningitis based on any etiology other than cryptococcosis. * History of allergy to or intolerance of imidazoles, or amphotericin B. * Moderate or severe liver disease defined as any one or more of the following: * SGOT or SGPT \> 5 x upper limit of normal, total bilirubin \> 2.5 mg/dl, prothrombin time \> 5 seconds over control, or alkaline phosphatase \> 2 x upper limit of normal. * Comatose patients. Concurrent Medication: Excluded: * Drugs with low therapeutic ratios that undergo hepatic metabolism may not be used with fluconazole until possible drug interactions have been clarified. * Coumarin-type anticoagulants. * Oral hypoglycemics. * Barbiturates. * Immunostimulants. * Investigational drugs or approved (licensed) drugs for investigational indications. * Systemic antifungal agent other than the assigned study drug. Concurrent Treatment: Excluded: Lymphocyte replacement. Prior Medication: Excluded within 4 weeks of study entry: * More than 1 mg/kg/week amphotericin B. Patients unlikely to survive more than 2 weeks.

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 6 ubicaciones

Suspendido

Univ of Miami School of Medicine

Miami, United StatesAbrir Univ of Miami School of Medicine en Google Maps
Suspendido

Tulane Univ School of Medicine

New Orleans, United States
Suspendido

Mem Sloan - Kettering Cancer Ctr

New York, United States
Suspendido

Bronx Municipal Hosp Ctr/Jacobi Med Ctr

The Bronx, United States
Completado6 Centros de Estudio