Randomized Study of Fluoxetine in Children and Adolescents With Autism
fluoxetine
Trastorno del Espectro Autista+6
+ Trastornos Generalizados del Desarrollo Infantil
+ Enfermedades del sistema nervioso
Estudio de Tratamiento
Resumen
Fecha de inicio: 1 de septiembre de 1998
Fecha en la que se inscribió al primer participante.PROTOCOL OUTLINE: This is a randomized, double blind, placebo controlled, crossover study. All patients receive oral placebo daily during week 0. Patients are randomized to receive either oral fluoxetine or oral placebo daily on weeks 1-8. Patients then crossover to receive treatment on the other arm during weeks 12-20. Completion date provided represents the completion date of the grant per OOPD records
Protocolo
Esta sección proporciona detalles del plan del estudio, incluyendo cómo está diseñado y qué se está evaluando.Se reclutarán 45 pacientes
Número total de participantes que el ensayo clínico espera reclutar.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.De 5 a 17 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
PROTOCOL ENTRY CRITERIA: --Disease Characteristics-- Meets diagnostic criteria for autism --Prior/Concurrent Therapy-- Other: At least 3 months since prior electroconvulsive therapy At least 1 month since prior investigational drugs or treatment with any drug known to cause major organ toxicity At least 2 weeks since prior monoamine oxidase inhibitors At least 6 weeks since prior long acting phenothiazines At least 1 week since prior other psychotropic drugs No prior fluoxetine of 20 mg/day for 6 weeks At least 6 weeks since prior fluoxetine No concurrent use of terfenadine (Seldane) or astemizole (Hismanal) No concurrent electroconvulsive therapy or other psychotropic drugs (unless otherwise permitted) Prior participation in another serotonin reuptake inhibitor trial allowed --Patient Characteristics-- Hematopoietic: No significant hematopoietic disease Hepatic: No prior or concurrent liver disease Renal: No prior or concurrent kidney disease Cardiovascular: No significant cardiovascular disease No abnormal EKG Neurological: No prior seizure disorder or high risk development of seizures No prior cerebrovascular disease No prior brain trauma Other: Not pregnant or nursing Negative pregnancy test No unstable major medical illness or systemic disease No moderate or severe mental retardation and motor deficits (IQ less than 50) No family history of bipolar disorder No prior or concurrent other mental disorders (e.g., schizophrenia, schizoaffective, organic, or bipolar disorders) No significant autoaggressive behavior or serious suicidal risk No prior or concurrent gastrointestinal conditions No unstable endocrine disease (e.g., hypo or hyperthyroidism) No prior or concurrent malignancy Must be able to tolerate tapering of psychoactive medication No history of hypersensitivity or severe side effects to fluoxetine or other serotonin reuptake inhibitors No history of severe personality disorder or noncompliance
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 3 ubicaciones
New York University Medical Center
New York, United StatesAbrir New York University Medical Center en Google MapsMount Sinai School of Medicine
New York, United StatesAlbert Einstein College of Medicine
The Bronx, United States