Comparative Study Between the AirGoTM System and Standard Tests in the Assessment of the Respiratory Function
NCT ID: NCT03368612
Last Updated: 2017-12-11
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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UNKNOWN
100 participants
OBSERVATIONAL
2017-09-22
2019-09-22
Brief Summary
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Detailed Description
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• 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
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Study Design
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COHORT
PROSPECTIVE
Interventions
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Electronic evaluation system
spirometry, plethysmography, cardiopulmonary exercise test
Electronic evaluation system
AirGo recording
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
* Able to perform a routine respiratory function test (spirometry and cardiopulmonary exercise testing),
* aged between 18 and 75 years,
* who signed a written informed consent.
Exclusion Criteria
* History of coronary artery disease or heart failure;
* Respiratory comorbidities (eg. asthma, chronic obstructive disease, sleep apnoea, lung interstitial disease);
* Pregnancy;
* Former smoker of \>5 p/y;
* Severe trauma or major surgery in the last year;
* Chest pain;
* Obesity (BMI \>30).
18 Years
75 Years
ALL
Yes
Sponsors
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Ospedale Santa Croce-Carle Cuneo
OTHER
Responsible Party
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Andrea Antonelli
Principal Investigator, MD
Locations
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A.O. S. Croce E Carle Di Cuneo
Cuneo, , Italy
Countries
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Central Contacts
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Facility Contacts
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FRANCESCO GIURLANDA
Role: primary
Other Identifiers
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A.O. S. Croce e Carle di Cuneo
Identifier Type: -
Identifier Source: org_study_id