Early breathing therapy just one hour after CABG extubation
Official title: Early Postoperative Physiotherapy in the Prevention Respiratory Insufficiency After Elective Heart Surgery
Run by Alma Mater Europaea - Slovenia · NCT07730034 · Data updated 2026-11-12
This trial tests whether starting respiratory physiotherapy one hour after extubation improves recovery for adults after elective CABG compared with starting on the first postoperative day.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 18 Years to 80 Years |
| Sex | All |
| Enrollment | 40 (estimated) |
| Sponsor | Alma Mater Europaea - Slovenia Academic / other |
| Locations | 1 site (Zagreb) |
| Status | Recruiting |
| Started | August 4, 2026 |
| Main results expected | May 2027 |
| Study ends | June 2027 |
| Registry record updated | August 12, 2026 |
| Trial ID | NCT07730034 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Adults 18–80 years old undergoing elective CABG, extubated on postoperative day 0, with BMI <30 kg/m² and EF >25%.
✕Probably not a fit
Patients not extubated on POD 0 or with significant exclusion criteria may not benefit or be eligible.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
Adults undergoing elective CABG are randomized to receive respiratory physiotherapy either one hour after extubation or starting the following postoperative day. The study aims to see if earlier therapy improves lung function, reduces lung-related complications, shortens ICU and hospital stays, and eases pain and anxiety. It uses standardized physiotherapy procedures and perioperative care to ensure consistent assessment. Conducted at University Hospital Centre Zagreb, the trial follows good clinical practice and ethical guidelines.
Why it matters
Potential benefit: If successful, patients could recover faster with fewer breathing-related complications and shorter ICU/hospital stays.
How similar studies have gone: Prior studies recognize early respiratory therapy as helpful, but the optimal timing remains unclear and this trial tests a very early initiation.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Adults aged 18-80 years * Male and female participants * Elective coronary artery bypass grafting (CABG) * Body mass index (BMI) \< 30 kg/m² * Left ventricular ejection fraction (EF) \> 25% * Extubated on postoperative day 0 (POD 0) * Able and willing to provide written informed consent * Able to perform spirometry and follow study instructions Exclusion Criteria: * Refusal or inability to provide informed consent * Emergency CABG surgery * Previous cardiac surgery * Severe cardiac arrhythmias (e.g., ventricular tachycardia/fibrillation, third-degree atrioventricular block) * Previous stroke * Motor impairment of upper or lower extremities due to neurological or musculoskeletal disease * Dyskinesia * Not extubated on POD 0 * Significant postoperative neurological complications * Peripheral arterial disease of the lower extremities or previous lower-limb amputation * Acute or chronic pulmonary disease * Preoperative FEV1 \<30% of predicted (greater than 70% reduction) * Inability to perform spirometry correctly * Cancelled surgery after preoperative assessment * Extubation later than 24 hours after surgery * Requirement for continuous positive airway pressure (CPAP) after extubation SpO₂ \<90% one hour after extubation despite oxygen supplementation (4 L/min by nasal cannula) * Return to the operating room after the initial CABG procedure * Requirement for dialysis (acute or chronic)
Where it's running
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University Hospital Centre Zagreb
Zagreb, Croatia Recruiting
Study contacts
- Principal investigator: Dijana Filipović, MSc — Clinical Hospital Centre Zagreb
- Study coordinator: Dijana Filipović, MSc
- Email: dijana.filipovic@kbc-zagreb.hr
- Phone: +385 99 4663124
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.