Completado

Trial of Inspiratory Muscle Rest and Exercise in Chronic Obstructive Lung Disease

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

ventilators, negative pressure

Dispositivo
Quiénes están siendo reclutados

Lung Diseases

+ Lung Diseases, Obstructive
+ Chronic Obstructive Pulmonary Disease
De 30 a 75 años
Cómo está diseñado el estudio

Estudio de Tratamiento

Fase 3
Intervencional
Inicio del estudio: febrero de 1986

Resumen

Patrocinador PrincipalMcGill University
Última actualización: 29 de diciembre de 2015
Extraido de una base de datos validada por el gobierno.Reclamar como socio
Fecha de inicio: 1 de febrero de 1986Fecha en la que se inscribió al primer participante.

To test the effectiveness of ventilatory muscle rest (VMR) using home negative pressure ventilation (NPV) in improving exercise performance, alleviating dyspnea, and improving the quality of life in patients with severe chronic obstructive lung disease. BACKGROUND: The potential importance of respiratory, chiefly inspiratory-muscle, fatigue had only recently been appreciated. If inspiratory muscles fail, so does ventilation and tissue respiration. There are theoretical reasons to postulate inspiratory muscle failure in chronic obstructive pulmonary disease, and suggestions that it may occur in an acute form with exacerbations and in a chronic form during 'stability'. There are two therapeutic strategies available for prevention and treatment of inspiratory muscle fatigue: training inspiratory muscles to increase their efficiency and resting fatigued muscles. The former should work if chronic fatigue is not present, and the latter should allow recovery from chronic fatigue, so the two approaches are not necessarily mutually exclusive. This proposal was originally designed to test the efficacy of each of these therapies alone and also in combination; however, given the experience of a pretrial period, these goals were scaled back. Since there was reason to believe that VMR may be more effective than IMT, the trial focused on VMR and sham VMR only. Ventilatory muscle rest was applied using a negative pressure ventilation suit sealed at the patient's hips, arms, and neck. A widebore tube connected to a fitting in the suit above the grid on the chest and upper abdomen transmitted negative pressure to the chest wall from the pump, thereby inflating the lungs. The evidence for chronic inspiratory muscle fatigue in patients with COLD resided largely in several relatively poorly controlled studies indicating that nocturnal artificial ventilation, which presumably rested the inspiratory muscles, produced improvement in daytime function and blood gases. The trial produced some badly needed data on both the occurrence of inspiratory muscle fatigue in COLD patients and its treatment with VMR. DESIGN NARRATIVE: Randomized, blinded. A total of 1,231 patients in the metropolitan Montreal area were screened. Of these, 348 were recruited to enter a four week stabilization period, and 184 were subsequently randomized to either active or sham negative pressure ventilation (NPV). A five day in-hospital period was used to train patients in ventilator use and obtain baseline measures of exercise capacity, lung function, respiratory symptoms, and quality of life. Randomization was stratified on the basis of whether or not the patient had been receiving oxygen at home. Home ventilation treatment took place during a following 12-week period. Respirator use was recorded from patient logs and from concealed meters installed in the units. Patients received four home visits by physiotherapists during the 12-week period and returned to the hospital for follow-up at four and twelve weeks post-discharge for reassessment. The principal outcome measure was the distance in meters walked in six minutes. Secondary outcome measures were cycle exercise endurance time, severity of dyspnea, quality of life, arterial blood gas tensions, and respiratory muscle strength.

Título OficialTrial of Inspiratory Muscle Rest and Exercise in Chronic Obstructive Lung Disease 
Patrocinador PrincipalMcGill University
Última actualización: 29 de diciembre de 2015
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
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.

Cómo se asignan los participantes a diferentes grupos/brazos
En este estudio clínico, los participantes se colocan en grupos de forma aleatoria, como si se lanzara una moneda. Esto garantiza que el estudio sea justo e imparcial, lo que hace que los resultados sean más confiables. Al asignar a los participantes al azar, los investigadores pueden comparar mejor los tratamientos sin influencias externas.

Otras formas de asignar participantes
Asignación no aleatoria
: Los participantes se asignan en función de factores específicos, como su condición médica o la decisión de un médico.

Ninguna (ensayo de un solo brazo)
: Si el estudio tiene un solo grupo, todos los participantes reciben el mismo tratamiento y no se necesita asignación.

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.
De 30 a 75 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
Lung Diseases
Lung Diseases, Obstructive
Chronic Obstructive Pulmonary Disease
Criterios

No eligibility criteria



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 no tiene datos de ubicaciónNo hay información disponible sobre las ubicaciones de este estudio. 

CompletadoNingun centro de estudio