An Open-Label, Randomized, Three-Arm, Comparative Trial of a Caloric Supplement With Peptides and Medium-Chain Triglycerides Versus a Caloric Supplement With Whole Protein and Long-Chain Triglycerides Versus No Caloric Supplement for the Prevention of Weight Loss in Individuals With AIDS Who Take a Daily Multivitamin and Mineral Supplement
Datos de Suplemento Dietético
+ dietarySupplement Data
+ dietarySupplement Data
Recopilados desde hoy en adelante - ProspectivoInfecciones Transmitidas por la Sangre+20
+ Enfermedades Urogenitales
+ Enfermedades Genitales
Cohorte
Seguimiento de la incidencia de una enfermedad para identificar factores de riesgo y comprender su progresión a lo largo del tiempo.Resumen
Fecha de inicio: 1 de junio de 1996
Fecha en la que se inscribió al primer participante.Patients will be randomized to one of 3 study arms: Arm 1 - Peptamen drinks + multivitamin and mineral supplement, taken in addition to regular diet for 4 months Arm 2 - NuBasics drinks or equivalent amounts of NuBasics soups or bars + multivitamin and mineral supplement, taken in addition to regular diet for 4 months Arm 3 - Multivitamin and mineral supplement, taken in addition to regular diet for 4 months. At months 0, 2, and 4, patients will be assessed for weight, body cell mass, patient-reported physical activity level, and dietary intake (by 24-hour dietary recall). At months 2 and 4, they will also be assessed for compliance with study regimen. Patients who complete their 4 month follow up visit will be provided with a 30 day supply of the caloric supplement of their choice (Peptamen or NuBasics) and a 30 day supply of the study multivitamin supplement.
Protocolo
Esta sección proporciona detalles del plan del estudio, incluyendo cómo está diseñado y qué se está evaluando.Se reclutarán 536 pacientes
Número total de participantes que el ensayo clínico espera reclutar.Cohorte
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: HIV infection. Stable weight. CD4+ cell count <200 cells/mm3. Life expectancy of at least 6 months. Parent or legal guardian to sign written, informed consent for patients < 18 years old. Exclusion Criteria Co-existing Condition: Patients with any of the following symptoms or conditions are excluded: Active opportunistic infection, requiring acute treatment. Malignancy (other than stable cutaneous Kaposi's sarcoma that does not require systemic chemotherapy). Diabetes mellitus or other conditions requiring special dietary restrictions. Body mass index (BMI) >= 29.0 kg/m2. Disorders or conditions that, in the treating clinician's opinion, may prevent adequate compliance with protocol requirements. Concurrent Medication: Excluded: Growth hormone. Megestrol acetate (Megace). Cyproheptadine (Periactin). Dronabinol (Marinol). Thalidomide. Anabolic steroids (e.g., nandrolone decanoate)(Deca-durabolin). Pharmacologic-dose corticosteroids (e.g., > 15 mg/day prednisone equivalent) NOTE: Men requiring testosterone replacement therapy for documented hypogonadism may be enrolled. Caloric nutritional supplements deemed by the clinician to promote weight gain or maintenance. Patients with the following prior condition are excluded: History of phenylketonuria. Prior Medication: Excluded within the past 2 weeks: Use of caloric nutritional supplements for more than 5 days deemed by the clinician to promote weight gain or maintenance. Excluded within the past 30 days: Growth hormone. Megestrol acetate (Megace). Cyproheptadine (Periactin). Dronabinol (Marinol). Thalidomide. Anabolic steroids (e.g., nandrolone decanoate)(Deca-durabolin) Pharmacologic-dose corticosteroids (e.g., > 15 mg/day prednisone equivalent). NOTE: Men requiring testosterone replacement therapy for documented hypogonadism may be enrolled.
Plan de Estudio
Conoce todos los tratamientos administrados en este estudio, su descripción detallada y en qué consisten.3 grupos de intervención están designados en este estudio
0% de probabilidad de ser asignado al grupo placebo
Grupos de Tratamiento
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 17 ubicaciones
Community Consortium / UCSF
San Francisco, United StatesAbrir Community Consortium / UCSF en Google MapsDenver CPCRA / Denver Public Hlth
Denver, United StatesWashington Reg AIDS Prog / Dept of Infect Dis
Washington D.C., United StatesAIDS Research Consortium of Atlanta
Atlanta, United States