Breathing exercises and triflow device effects on recovery after heart surgery
Comparison of the Effects of Triflow and Deep Breathing and Cough Exercises on Postoperative Respiratory Functions in Patients Undergoing Mitral Valve Replacement: A Randomized Controlled Trial
This study tests whether combining breathing exercises with a triflow device helps patients recover better after mitral valve replacement surgery compared to using the triflow device alone.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 60 (estimated) |
| Ages | 18 Years to 80 Years |
| Sex | All |
| Sponsor | Atlas University Academic / other |
| Locations | 2 sites (Istanbul and 1 other locations) |
| Trial ID | NCT06997224 on ClinicalTrials.gov |
What this trial studies
This study investigates the impact of breathing exercises and the triflow device on respiratory function in patients who have undergone mitral valve replacement surgery. It aims to compare the effectiveness of using triflow alone versus triflow combined with deep breathing and cough exercises. The research addresses the high incidence of lung complications following heart surgery, which can significantly affect recovery. By evaluating these methods, the study seeks to identify the best approach to enhance postoperative respiratory outcomes.
Who should consider this trial
Good fit: Ideal candidates are patients undergoing mitral valve replacement surgery who are literate and can communicate in the native language.
Not a fit: Patients who are hemodynamically unstable or have developed postoperative respiratory complications will not benefit from this study.
Why it matters
Potential benefit: If successful, this study could improve respiratory recovery and reduce complications for patients after mitral valve replacement surgery.
How similar studies have performed: Previous studies on respiratory interventions post-surgery have shown mixed results, indicating that this approach may provide new insights into effective recovery strategies.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Volunteering to participate in the study Literate and knowing the native language Exclusion Criteria: * Hemodynamically unstable patients, Patients who develop postoperative respiratory complications, Lip or palate anomalies
Where this trial is running
Istanbul and 1 other locations
- Medipol Hospital — Istanbul, Turkey (Türkiye) (Recruiting)
- Medipol Hospital — Istanbul, Turkey (Türkiye) (Recruiting)
Study contacts
- Study coordinator: çağla toprak, dr
- Email: caykinn@gmail.com
- Phone: 532 799 78 14
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.