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Clinical Trial Summary

In this study the invetigators seek an answer on the following hypothesis:

- What are the long term effects of an IPV treatment evaluated with classical outcome parameters? (FEV1, Raw)

- Is the possible effect noticeable on the novel technique and is this comparable with the classical outcome parameters?


Clinical Trial Description

A Multicenter study conducted in university Hospital Antwerp (UZA) and ZNA Middelheim.

Tests are taken before and after one week IPV treatment. IPV is applied for 1 week during the physical therapy treatment of chronic obstructive pulmonary desease (COPD) patients admitted to the hospital for an excarebation. The IPV treatment is an additional treatment upon the standard treatment of the patients. The standard treatment consists out of existing drainage techniques to remove secretion out of the lungs by means of breathing control exercises. Patients are randomized into either the experimental group or the control group. The control group receives a standard physical therapy treatment without additional IPV treatment. ;


Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Double Blind (Subject, Caregiver, Outcomes Assessor), Primary Purpose: Treatment


Related Conditions & MeSH terms


NCT number NCT01671540
Study type Interventional
Source University Hospital, Antwerp
Contact Kris Ides, Msc
Phone 036418267
Email kris.ides@artesis.be
Status Recruiting
Phase N/A
Start date September 2011

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