Clinical Trials Directory

Trials / Completed

CompletedNCT00710463

Evaluation of the Role of Nocturnal Non-Invasive Ventilation in Pulmonary Rehabilitation

Status
Completed
Phase
Study type
Observational
Enrollment
80 (actual)
Sponsor
Deutsche Lungenstiftung e.V. · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

Hypothesis: Hospital based, comprehensive pulmonary rehabilitation of patients with COPD in GOLD stage IV can be optimized by application of nocturnal non invasive ventilation. This hypotheses shall be tested by an observational trial, comparing rehabilitation effects of a prospectively observed group receiving non invasive ventilation, compared wiht a historical control group of patients who did received the same treatment without non invasive ventilation.

Detailed description

Non invasive ventilation is known to allow improvements if applied during endurance training, but this is technically difficult. Nocturnal application of non invasive ventilation is known to unload the ventilatory pump, reset the control of breathing, and improve sleep quality. The protocol also aimed to evaluate the acceptance of non invasive ventilation in patients undergoing a four week inpatient pulmonary rehabilitation programme.

Conditions

Interventions

TypeNameDescription
DEVICEnon invasive ventilation (Resmed VPAP III ST-A, Respironics Harmony)non invasive ventilation was performed with commercially available ventilators from the manufacturers Resmed and Respironics.

Timeline

Start date
2003-05-01
Primary completion
2007-09-01
Completion
2007-11-01
First posted
2008-07-04
Last updated
2008-07-04

Locations

1 site across 1 country: Germany

Source: ClinicalTrials.gov record NCT00710463. Inclusion in this directory is not an endorsement.