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Clinical Trial Summary

The purpose of this trial ist to investigate the difference of the efficacy of two systems for breath support in patients with COPD.


Clinical Trial Description

The trial consists of 12 weeks of therapy that is divided into two sections. In the first 6-week section patients receive treatment with either TNI or BiPAP and in the second 6-week section treatment is changed. The starting therapy is allocated to the patients via randomisation and should be started directly after the baseline visit.

The treatment and the follow-up period end with the second visit after the second treatment section and the patient decides which device he/she wants to use further. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02007772
Study type Interventional
Source University of Leipzig
Contact
Status Completed
Phase N/A
Start date June 2011
Completion date July 2017

See also
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