Male/female adults
Conditions
Interventions
None listed
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1. Healthy Japanese males and females aged 20 to 64 years old when informed consent. 2. Subjects who can give informed consent to partake in this research, after being provided with an explanation of the protocol detail.
Exclusion criteria
Exclusion criteria: 1. Subjects using beta-blockers, steroids, or beta2 agonists (bronchoconstrictors and bronchodilators). 2. Subjects with the following medical history or comorbidities: History of thoracic or abdominal surgery Myocardial infarction or angina pectoris Uncontrolled hypertension (Grade III or higher) 3. Subjects who cannot remove nail polish or artificial nails on the day of the examination. 4. Subjects planning to participate in another clinical trial between the date of consent and the examination visit. 5. Subjects deemed unsuitable for participation in the trial by the principal investigator or sub-investigator.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Systolic blood pressure, diastolic blood pressure, pulse rate, respiratory rate Respiratory function tests (SpO2, vital capacity (VC), forced vital capacity (FVC)) Acquisition of photo/video data | — |
Countries
Japan
Contacts
CPCC Company Limited Clinical Planning Department