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A Study to Evaluate the Effect of Anti-HIV Therapy on Lean Tissue (Muscle) in HIV-Positive Patients

0 criterios cumplidosConsulta de un vistazo cómo tu perfil cumple con cada criterio de elegibilidad.
Qué se está recopilando

Recolección de datos

Quiénes están siendo reclutados

HIV Infections

A partir de 18 años
Cómo está diseñado el estudio

Historia Natural

Observación de la progresión de una enfermedad en personas no tratadas para comprender su curso y resultados típicos.
Observacional

Resumen

Patrocinador PrincipalNational Institute of Allergy and Infectious Diseases (NIAID)
Última actualización: 24 de junio de 2005
Extraido de una base de datos validada por el gobierno.Reclamar como socio

The purpose of this study is to determine whether HIV-positive patients with extremely low viral loads (level of HIV in the blood) have a greater gain in lean tissue during anti-HIV (antiretroviral) therapy than patients with higher viral loads. Many HIV-positive patients experience changes in body composition (muscle, fat, etc.) while on antiretroviral therapy. However, any weight gained while taking antiretrovirals is mostly fat. A patient's viral load may affect whether weight gained is a result of increased fat or increased muscle. A large-scale study is needed to closely evaluate the effects of antiretroviral therapy on body composition. Effective antiretroviral therapy, as measured by a decrease in HIV-1 RNA levels, may sustain or improve important components of body composition, perhaps through a decrease in the underlying pro-inflammatory activity and resting energy expenditure. Moderate weight gain has been reported to be associated with HAART. Meaningful increase in total body weight, however, may need to be comprised of augmentation of lean body mass (primarily muscle), since mortality in HIV and cancer wasting is associated with sizable decreases in lean body mass (LBM) and there is no evidence that increases in fat cell mass are protective. To date, there has not been any large-scale prospective evaluation of the effects of HAART on body composition. Nor has it been determined whether increasing body weight or specific components of body composition (fat or lean body mass) in persons who have lost substantive amounts of weight protects against AIDS-defining complications or prolongs survival. This is a 48-week, observational study of lean body mass, appetite, functional performance, and systemic markers of inflammation during highly active antiretroviral therapy (HAART) in patients co-enrolled in ACTG antiretroviral studies. Patients are stratified by body mass index (BMI) into 2 cohorts: less than 23 kg/m2 versus greater than or equal to 23 to 28 kg/m2. At selected study visits, times of antiretroviral medication change, and following the diagnosis of an AIDS-defining event, the following are assessed: height (screening visit only), weight, lean body mass, appetite (by questionnaire), functional performance (by questionnaire), and markers of systemic inflammation.

Título OficialEffect of Highly Active Antiretroviral Therapy (HAART) on Lean Body Mass 
Patrocinador PrincipalNational Institute of Allergy and Infectious Diseases (NIAID)
Última actualización: 24 de junio de 2005
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 200 pacientesNúmero total de participantes que el ensayo clínico espera reclutar.
Historia Natural
Estos estudios observan la progresión de una enfermedad sin tratamiento activo, ayudando a entender cómo se desarrolla, cambia y afecta la calidad de vida con el tiempo.

Elegibilidad

Los investigadores buscan pacientes que cumplan ciertos criterios, conocidos como criterios de elegibilidad: estado general de salud o tratamientos previos.
Condiciones
Criterios
Cualquier sexoSexo biológico de los participantes elegibles para inscribirse.
A partir de 18 añosRango de edades de los participantes que pueden unirse al estudio.
Voluntarios sanos no permitidosIndica si personas sanas, sin la condición que se estudia, pueden participar.
Condiciones
Patología
HIV Infections
Criterios

Inclusion Criteria Patients may be eligible for this study if they: * Are enrolled in an adult AIDS clinical trial. * Are HIV-positive. * Have a viral load of at least 10,000 copies/ml. * Are expected to live at least 6 months. * Are at least 18 years old. Exclusion Criteria Patients will not be eligible for this study if they: * Have a history of diabetes requiring medication. * Have a history of heart disorders. * Have a fever, diarrhea, nausea, or a condition which makes it difficult to eat within the 14 days prior to study entry. * Have swelling due to any cause. * Are pregnant or breast-feeding. * Are receiving any therapy to increase your appetite or gain weight within 30 days prior to study entry. * Are receiving any therapy for a severe infection or medical illness within 14 days prior to study entry. * Are taking certain medications.



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 21 ubicaciones
Suspendido
Univ of Southern California / LA County USC Med CtrLos Angeles, United StatesVer ubicación
Suspendido
Univ of California / San Diego Treatment CtrSan Diego, United States
Suspendido
Stanford at Kaiser / Kaiser Permanente Med CtrSan Francisco, United States
Suspendido
Stanford Univ Med CtrStanford, United States

Completado21 Centros de Estudio