Effects of novel digital incentive spirometer device in patients with open heart surgery

Status

Active, not recruiting

Phases

Phase 1Phase 2

Study type

Interventional

Source

TCTR

Registry ID

TCTR20230921002

Enrollment

Registered

2023-09-21

Start date

2023-10-16

Completion date

Unknown

Last updated

2026-03-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

open heart surgery breathing exercise spirometer device pulmonary function respiratory muscle strength open heart surgery

Interventions

Digital device ,standard treatment: triflow

Experimental Device,No Intervention Device

Digital spirometer device,control group

Eligibility

Sex/Gender

All

Age

35 Years to 80 Years

Inclusion criteria

Inclusion criteria: open heart surgery diagnosed with coronary heart disease or valvular disease

Exclusion criteria

Exclusion criteria: aortic anueysm pregnacy

Design outcomes

Primary

Measure	Time frame
pulmonary performance at the beginning of study, at 3rd and 5th after extubation pulmonary function	—

Secondary

Measure	Time frame
pulmonary performance at the beginning of study, at 3rd and 5th after extubation performance respiratory muscle strength	—

Countries

Thailand

Contacts

Public ContactKornanong Yuenyongchaiwat

Thammasat University

kornaong.y@allied.tu.ac.th0824521680

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Apr 4, 2026