Trials / Completed
CompletedNCT02007772
Effectiveness of TNI vs. BiPAP in Chronic Global Insufficiency in COPD Patients
Effectiveness of TNI (Nasal High-flow) vs. BiPAP (Biphasic Positive Airway Pressure) in Chronic Global Insufficiency in COPD (Chronic Obstructive Pulmonary Disease) Patients
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 105 (actual)
- Sponsor
- University of Leipzig · Academic / Other
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
The purpose of this trial ist to investigate the difference of the efficacy of two systems for breath support in patients with COPD.
Detailed 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.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | nHF | nasal high-flow is used over a period of 6 weeks (outpatient) |
| DEVICE | BiPAP | BiPAP is used over a period of 6 weeks (outpatient) |
Timeline
- Start date
- 2011-06-01
- Primary completion
- 2017-07-01
- Completion
- 2017-07-01
- First posted
- 2013-12-11
- Last updated
- 2018-11-15
Locations
14 sites across 1 country: Germany
Source: ClinicalTrials.gov record NCT02007772. Inclusion in this directory is not an endorsement.