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Clinical Trial Summary

The purpose of this study is analyzed the impact of oxygen adjusted during exercise in COPD patients without conventional for LTOT but with exercise desaturation.


Clinical Trial Description

Oxygen will be administered through nasal cannulae. Patients will be provided with a tank of liquid oxygen and a rechargeable portable device. The 6 minuts walking test will be used to adjusted oxygen flow in the GFA group (to achieve a mean SpO2 ≥ 90%). In the control group (GC), a 3L/min oxygen flow will be administer. Oxygen is used when the patient perform physical activity. The treatment period for each patient is 6 months (3 months in the GC grup, 3 months in the GFA one). ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02273830
Study type Interventional
Source Hospital de Granollers
Contact
Status Completed
Phase Phase 4
Start date September 2015
Completion date October 2017

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