Recruiting

Observational Study

Sponsor:

Brigham and Women's Hospital

Code:

NCT07173998

Conditions

Postoperative Atrial Fibrillation

Eligibility Criteria

Sex: All

Age: 18 - 70+

Healthy Volunteers: Not accepted

Interventions

Survey

Study Details

Brief summary:

Prospective observational study on quality of life with postoperative atrial fibrillation after cardiac surgery using SF-36 and qualitative questions

Conditions

Postoperative Atrial Fibrillation

Study ID

NCT07173998

Start date

Jul 15, 2025

Status verified date

Jun, 2026

Completion date

Jul 1, 2027

Anticipated

Primary completion date

Dec 31, 2026

Anticipated

Eligibility Criteria

Eligibility Criteria

Sex: All

Age: 18 - 70+

Healthy Volunteers: Not accepted

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

Study Design

Enrollment

260 participants

Anticipated

Interventions and Outcome Measures

Arms

Target group

Adult patients undergoing cardiac surgery with cardiopulmonary bypass

Interventions

Survey

SF-36, TSQM-9, qualitative questions

Primary outcome measure

  • SF-36 scores [ Time Frame: before, one month and three months postop ]

Central Contacts and Locations

Central contacts

Locations

Mass General Brigham

Recruiting

Boston, Massachusetts, United States, 02115

Contacts

Jakob Wollborn, MD

jwollborn@bwh.harvard.edu

More Information

Sponsor

Brigham and Women's Hospital

Last update posted

Jun 29, 2026

Last verified

Jun, 2026

Keywords

  • cardiac surgery
  • recovery

Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-10. This information was provided to ClinicalTrials.gov by Brigham and Women's Hospital on 2026-06-29.