Clinical trial Recruiting at 1 site Observational Ages 18 and up

Assessing right atrial strain to predict postoperative atrial fibrillation after heart surgery

Official title: Predictive Value of Right Atrial Strain in Postoperative Atrial Fibrillation in Patients Undergoing Cardiac Surgery

Run by Centre Hospitalier Universitaire, Amiens · NCT06054360 · Data updated 2026-11-12

This study is testing if measuring right atrial strain can help predict the risk of developing atrial fibrillation after heart surgery in adults.

Quick facts

Study typeObservational
Ages18 Years and up
SexAll
Enrollment334 (estimated)
SponsorCentre Hospitalier Universitaire, Amiens
Academic / other
Locations1 site (Amiens)
StatusRecruiting
StartedOctober 9, 2023
Main results expectedOctober 9, 2026
Study endsOctober 9, 2026
Registry record updatedMay 28, 2026
Trial IDNCT06054360 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates are adults over 18 years old scheduled for aortocoronary bypass grafting at the Amiens University Hospital.

Probably not a fit

Patients with a history of atrial fibrillation or flutter, urgent cardiac surgery needs, or significant tricuspid insufficiency may not benefit from this study.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This observational study aims to investigate the predictive value of right atrial strain (RAS) in patients undergoing scheduled aortocoronary bypass grafting. By utilizing transthoracic echocardiography, the study will measure RAS parameters to determine their association with the occurrence of postoperative atrial fibrillation (POAF). Given that POAF can lead to serious complications, understanding the role of right atrial function may provide insights into patient outcomes following cardiac surgery. The study will include adult patients hospitalized at the Amiens University Hospital for this specific surgical procedure.

Why it matters

Potential benefit: If successful, this study could help identify patients at higher risk for postoperative atrial fibrillation, allowing for targeted interventions to improve outcomes.

How similar studies have gone: Previous studies have shown a correlation between right atrial function and postoperative atrial fibrillation, suggesting that this approach may yield valuable insights.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Adult patient (\>18 years old)
* The patient was hospitalized at the Amiens University Hospital for scheduled aortocoronary bypass grafting under cardiopulmonary bypass.
* Echocardiographic image quality enabling the measurement of RAS parameters
* Patient affiliation to a social security scheme
* Patient/proxy information and collection of their non-opposition.

Exclusion Criteria:

* Patients participating in an interventional study may modify the incidence of POAF.
* History of atrial fibrillation or flutter.
* Valvular and ascending aorta cardiac surgery
* Urgent cardiac surgery.
* Presence of tricuspid insufficiency greater than grade 2.
* Left ventricular ejection fraction lower than 50%.
* Patient receiving circulatory mechanical assistance before surgery.
* Dependency on ventricular and atrial pacing by an internal or external cardiac pacemaker during the echocardiographic examination.

Where it's running

  • CHU Amiens Picardie
    Amiens, France
    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.