Clinical trial Recruiting at 1 site Observational Ages 18 to 100

Quality of life after atrial fibrillation following heart surgery

Official title: Prospective Observational Study on Quality of Life With Postoperative Atrial Fibrillation

Run by Brigham and Women's Hospital · NCT07173998 · Data updated 2026-11-12

This project will see how atrial fibrillation that starts after heart surgery affects quality of life in adults having cardiac operations.

More Atrial Fibrillation trials

Quick facts

Study typeObservational
Ages18 Years to 100 Years
SexAll
Enrollment260 (estimated)
SponsorBrigham and Women's Hospital
Academic / other
Locations1 site (Boston, Massachusetts)
StatusRecruiting
StartedJuly 15, 2025
Main results expectedDecember 31, 2026
Study endsJuly 1, 2027
Registry record updatedJune 29, 2026
Trial IDNCT07173998 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Adults aged 18–99 scheduled for non-emergent cardiac surgery who can complete surveys and do not have persistent or preoperative atrial fibrillation are ideal candidates.

Probably not a fit

People with persistent or preexisting atrial fibrillation, those presenting in atrial fibrillation before surgery, patients having emergent operations, or those unable to complete questionnaires are unlikely to benefit from this project.

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

What this trial studies

This is a prospective observational project that follows adults scheduled for cardiac surgery who develop postoperative atrial fibrillation. Participants complete baseline surveys before surgery and follow-up surveys at one month and three months after the operation using the SF-36, TSQM-9, and open-ended questions. The design captures short-term changes in health-related quality of life and treatment satisfaction without introducing new treatments. Patients with persistent or preoperative atrial fibrillation and those undergoing emergent operations are excluded.

Why it matters

Potential benefit: If successful, the findings could help clinicians better understand recovery after postoperative atrial fibrillation and tailor follow-up care to improve patients' quality of life.

How similar studies have gone: Prior observational work links postoperative atrial fibrillation to worse short-term outcomes and reduced quality of life, but prospective surveys at 1 and 3 months are relatively limited, so this approach builds on but also fills gaps in existing evidence.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* All genders
* Ages 18-99 years old
* Scheduled to undergo cardiac surgery
* Able to answer survey questions

Exclusion Criteria:

* Persistent / permanent atrial fibrillation
* Atrial fibrillation at presentation for surgery
* Emergent operations

Where it's running

  • Mass General Brigham
    Boston, Massachusetts, United States
    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.