healthy male adults
Conditions
Interventions
The spirometry using the wearable spirometer will be performed in addition to a routine spirometry, and the results will be compared under the resting condition, the exercise tolerance with 10 min wal
Sponsors
Department of Pathophysiological Laboratory Sciences Nagoya University Graduate School of Medicine
Eligibility
Sex/Gender
Male
Inclusion criteria
Inclusion criteria: Healthy male adults aged 20 years or more Those who is able to read and understand the Informed Consent Form and will sign the Informed Consent.
Exclusion criteria
Exclusion criteria: Those who feel uncomfortable during the study Those who are judged inappropriate for the cooperation of this study by the investigator in charge
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| spirometry percutaneous oxygen saturation | — |
Secondary
| Measure | Time frame |
|---|---|
| Questionnaire (height, body weight, history of smoking, impression of this examination) | — |
Countries
Japan
Contacts
Public ContactMiyoko Matsushima
Nagoya University Graduate School of Medicine Department of Pathophysiological Laboratory Sciences
Outcome results
None listed