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Clinical Trial Summary

The aim of the study is to compare the efficacy of using EFA technology versus the combination of EFA + high flow in hypersecretory patients COPD and bronchiectasis


Clinical Trial Description

After being informed about the study and potential risks, all patients giving written informed consent will undergo a 13-weeks trial period: 6 weeks of one technology (EFA / EFA+ HIGH FLOW), 1- wash out week and 6- weeks of the other technology in a cross over randomized trial. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06017739
Study type Interventional
Source Azienda Socio Sanitaria Territoriale della Valle Olona
Contact Marianna Messina
Phone +393356509059
Email annamessina.mm@gmail.com
Status Recruiting
Phase N/A
Start date October 9, 2023
Completion date January 18, 2025

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