Niaspan and Statin vs. Other Lipid-Modifying Therapies for Dyslipidemia
Colección de datos
Enfermedades Oclusivas Arteriales+12
+ Trastornos Cerebrovasculares
+ Enfermedades del Sistema Nervioso Central
Estudio de Tratamiento
Resumen
Fecha de inicio: 1 de abril de 2004
Fecha en la que se inscribió al primer participante.This study is about comparing the effectiveness of different treatments for dyslipidemia, a condition where there are high levels of cholesterol or fats in the blood. The treatments being compared include a combination of Niaspan and atorvastatin, a combination of simvastatin and ezetimibe, rosuvastatin alone, and a combination of Niaspan and rosuvastatin. The goal is to see which of these treatments works best for managing dyslipidemia. This study is important for adults aged 21 years and older who are eligible for treatment based on the National Cholesterol Education Program Adult Treatment Panel III recommendations and have triglycerides levels less than or equal to 300 mg/dL. The results of this study could help improve care for people with dyslipidemia by identifying the most effective treatment options. During this 12-week study, participants are randomly assigned to one of four treatment groups. In the first group, participants receive a combination of Niaspan and atorvastatin, with the doses adjusted to 2000 mg and 40 mg, respectively. The second group receives a combination of simvastatin, adjusted to 40 mg, and ezetimibe, maintained at 10 mg. The third group receives rosuvastatin alone, with the dose adjusted to 40 mg. The fourth group receives a combination of Niaspan and rosuvastatin, with the doses adjusted to 1000 mg and 20 mg, respectively. The study measures the change in LDL-C (low-density lipoprotein cholesterol, also known as 'bad' cholesterol) from the start to the end of the study to evaluate the effectiveness of each treatment.
Protocolo
Esta sección proporciona detalles del plan del estudio, incluyendo cómo está diseñado y qué se está evaluando.Se reclutarán 300 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.A partir de 21 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
Plan de Estudio
Conoce todos los tratamientos administrados en este estudio, su descripción detallada y en qué consisten.Objetivos del Estudio
Objetivos Primarios