NCT03368612

Comparative Study Between the AirGoTM System and Standard Tests in the Assessment of the Respiratory Function

• Status: Unknown
• Phase: —
• Study type: Observational
• Enrollment: 100 (estimated)
• Sponsor: Ospedale Santa Croce-Carle Cuneo · Academic / Other
• Sex: All
• Age: 18 Years – 75 Years
• Healthy volunteers: Accepted

Summary

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

Detailed 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).

Conditions

• Respiration Disorders

Interventions

Type	Name	Description
OTHER	Electronic evaluation system	spirometry, plethysmography, cardiopulmonary exercise test
OTHER	Electronic evaluation system	AirGo recording

Timeline

• Start date: 2017-09-22
• Primary completion: 2019-09-22
• Completion: 2019-09-22
• First posted: 2017-12-11
• Last updated: 2017-12-11

Locations

1 site across 1 country: Italy