Atrial Fibrillation Trial, Recruiting
Who may be able to join
AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI
Who might be able to join this trial:
- Adults aged 18 years or older
- People who need surgery on the upper part of the main blood vessel leaving the heart (the aorta), the heart valves, and/or the arteries that supply blood to the heart
- People who are able to give their written agreement to take part in the study
Who may not be able to join:
- People who have a history of irregular heart rhythms known as atrial fibrillation or atrial flutter
- People who have had previous heart surgery, are scheduled for minimally invasive heart surgery, or who need surgery urgently in an emergency situation
- People who require a procedure that involves cooling the body to very low temperatures to stop blood flow during surgery
- People who have a disease affecting the lining around the left lung, or who have previously had surgery through the left side of the chest
- People who have an abnormally shaped or deformed chest
- People who are unlikely to attend follow-up appointments after the study
Important: Always verify eligibility with the trial site directly before applying.
Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.
Contact this trial
Principal Investigator: Lin Han, M.D. Ph.D., Naval Medical University Changhai Hospital
Phone: 86-21-31161765
Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.
GP referral letter
Print a one-page summary to share with your doctor.
Trial details
Where this trial is recruiting
Primary endpoints
Postoperative atrial fibrillation
Can't join this trial?
Data last synced from ClinicalTrials.gov: 27 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.