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Clinical Trial Summary

The study aims at evaluating the AirGoTM system's performance, as compared to standard pulmonary function tests.


Clinical Trial Description

Primary endpoint:

• To test the AirGoTM system's respiratory rate recording accuracy at rest and during physical exercise, as compared to standard tests.

Secondary endpoints:

- To test the accuracy of the AirGoTM system's derived respiratory parameters (tidal volume, minute ventilation, Tiffeneau-Pinelli index, FEV1 and VO2max) at rest and during physical exercise, as compared to standard tests.

- To test comfort and subjects' compliance with the AirGoTM system during long term recording (24 hours). ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03368612
Study type Observational
Source Ospedale Santa Croce-Carle Cuneo
Contact ANDREA ANTONELLI, MD
Phone +39017161
Email ANTONELLI.A@OSPEDALE.CUNEO.IT
Status Recruiting
Phase N/A
Start date September 22, 2017
Completion date September 22, 2019

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