Quality of Life in Patients With Postoperative Atrial Fibrillation After Cardiac Surgery

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18-100
SponsorBrigham and Women's Hospital

About this trial

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

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

All genders

Ages 18-99 years old

Scheduled to undergo cardiac surgery

Able to answer survey questions

Disqualifiers

Persistent / permanent atrial fibrillation

Atrial fibrillation at presentation for surgery

Emergent operations

Trial population

Adult patients undergoing cardiac surgery with cardiopulmonary bypass

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

  • Survey

    Other intervention

    SF-36, TSQM-9, qualitative questions

Treatment groups

260 Participants
are divided into 1 treatment group
Group A: Target group1 intervention

Trial outcomes

Primary outcomes

1

SF-36 scores

compare development and absolut SF-36 scores

Time frame
before, one month and three months postop

Secondary outcomes

1

Qualitative questions

exploratory evaluation of qualitative questions

Time frame
before, one month and three months postop
2

TSQM-9 scores

TSQM-9 scores in Afib-patients

Time frame
one month and three months postop

Other outcomes

Sponsors and contacts

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