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Clinical Trial Summary

The goal of the study is to test the role of telemedicine combined with humidification to check CPAP treatment during the first month to improve adherence and reduce unsolved side effects of therapy.


Clinical Trial Description

The primary goal of OSAS therapy is to obtain CPAP adaptation for the highest amount of OSAS patients to reduce the proportion of untreated OSAS in the population. This object is important considering that a longer duration of CPAP treatment is linked with better daytime functioning and metabolic and blood pressure effects of CPAP. The main endpoints will be CPAP usage (defined as the proportion of night with CPAP usage ≥1h); CPAP adherence (defined as the proportion of night with CPAP usage ≥4h); the average nightly usage of CPAP (hour/night); CPAP efficacy (defined as AHI and ESS score). Each measure will be performed after 1 week, 1 month and 6 months. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04300166
Study type Interventional
Source Neuromed IRCCS
Contact Andrea Romigi, PhD
Phone +390865929636
Email andrea.romigi@neuromed.it
Status Not yet recruiting
Phase N/A
Start date June 1, 2020
Completion date June 1, 2022

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