Clinical trial Recruiting at 1 site Interventional Ages 18 to 80

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 typeInterventional
Ages18 Years to 80 Years
SexAll
Enrollment40 (estimated)
SponsorAlma Mater Europaea - Slovenia
Academic / other
Locations1 site (Zagreb)
StatusRecruiting
StartedAugust 4, 2026
Main results expectedMay 2027
Study endsJune 2027
Registry record updatedAugust 12, 2026
Trial IDNCT07730034 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

  • University Hospital Centre Zagreb
    Zagreb, Croatia
    Recruiting

Study contacts

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.