cardiovascular disease cardiovascular disease
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: This study targets individuals who meet all of the following criteria: 1) Individuals who are at least 140 cm in height at the time of consent acquisition (age is not considered). 2) Individuals who, after receiving a comprehensive explanation regarding participation in this study, have demonstrated a sufficient understanding and have provided written consent freely of their own volition. 3) A person who has obtained consent from a surrogate.
Exclusion criteria
Exclusion criteria: The following criteria will exclude individuals from participating in this study 1. Inability to perform measurements due to patient refusal or the following conditions Deformity of the chest History of thoracic surgery Recent surgical wounds, healing tissues, or recent skin grafts/ flaps on the chest Osteoporosis or osteomyelitis of the ribs Presence of pain in the chest wall Presence of implanted metal devices, such as pacemakers, between the ReDS Pro and the chest 2. Any other condition that the principal investigator or sub-investigators deem unsuitable for study participation
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Post-operative hospital stay | — |
Secondary
| Measure | Time frame |
|---|---|
| Number of complication events requiring treatment: heart failure, infection, vascular events | — |
Contacts
Okayama University