Actively Recruiting

Age: 18Years +
All Genders
NCT07434674

Incidence of Long-TeRm Atrial Fibrillation After Acute Illness

Led by University of California, San Diego · Updated on 2026-02-25

100

Participants Needed

1

Research Sites

108 weeks

Total Duration

On this page

Sponsors

U

University of California, San Diego

Lead Sponsor

B

Boston Scientific Corporation

Collaborating Sponsor

AI-Summary

What this Trial Is About

The investigators seek to conduct a prospective study to assess the recurrence of AF in patients with acute AF using a long-term ECG monitoring strategy with an insertable cardiac monitor (ICM), which is clinically indicated in this scenario as part of the standard of care. The investigators hypothesize that patients diagnosed with acute AF in the setting of cardiac surgery will have higher rates of AF recurrence than acute AF diagnosed in the setting of non-cardiac surgery or medical illness.

CONDITIONS

Official Title

Incidence of Long-TeRm Atrial Fibrillation After Acute Illness

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patient has an existing clinical indication for implantation of an insertable cardiac monitor (ICM) and will undergo ICM implantation as part of their standard medical care.
  • Patient is scheduled to receive or has received a Boston Scientific LUX-DX122; insertable cardiac monitor.
  • Episode of acute AF detected in an acute care setting or during an acute illness, confirmed by 12-lead ECG and 24-hour ECG or telemetry monitoring.
  • Patient or legally authorized representative signs and dates the patient consent form.
  • Patient is 18 years old or older.
  • Patient is willing and able to comply with all study procedures and attend the required follow-up visits for the duration of the study.
Not Eligible

You will not qualify if you...

  • Patient has a known history of AF or atrial flutter prior to the index acute AF episode.
  • Patient has another indication for antiarrhythmic medications independent of the acute AF episode.
  • Patient has a permanent contraindication to oral anticoagulation that would prevent future AF management with anticoagulants.
  • Patient is currently enrolled in another clinical trial affecting this study's objectives or endpoints.
  • Patient's life expectancy is less than one year.
  • Patient is pregnant.
  • Patient currently needs implantation of a cardiac implantable electronic device (CIED) or an implantable hemodynamic monitoring system.
  • Patient is not fit, able, or willing to follow the required study procedures.

AI-Screening

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Trial Site Locations

Total: 1 location

1

Sulpizio Cardiovascular Center

La Jolla, California, United States, 92037

Actively Recruiting

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Research Team

B

Benjamin U Hoffman, MD, PhD

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

1

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