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Clinical Trials/NCT07173998
NCT07173998RecruitingNot Applicable

Prospective Observational Study on Quality of Life With Postoperative Atrial Fibrillation

Brigham and Women's Hospital1 site in 1 country260 target enrollmentStarted: July 15, 2025Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Recruiting
Enrollment
260
Locations
1
Primary Endpoint
SF-36 scores

Study Overview

Brief Summary

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

Detailed Description

This is a prospective observational study on quality of life in patients after cardiac surgery with postoperative atrial fibrillation. Patients will answer surveys before their surgery as well as one and three months after their heart operation. The survey includes SF-36, TSQM-9 and qualitative questions.

Study Design

Study Type
Observational
Observational Model
Cohort
Time Perspective
Prospective

Eligibility Criteria

Ages
18 Years to 100 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

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

Arms & Interventions

Target group

Adult patients undergoing cardiac surgery with cardiopulmonary bypass

Intervention: Survey (Other)

Outcomes

Primary Outcomes

SF-36 scores

Time Frame: before, one month and three months postop

compare development and absolut SF-36 scores

Secondary Outcomes

  • Qualitative questions(before, one month and three months postop)
  • TSQM-9 scores(one month and three months postop)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Jakob Wollborn, MD

Principal Investigator

Brigham and Women's Hospital

Study Sites (1)

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