Observational Study on Long-Term Atrial Fibrillation After Acute Illness

This study is looking at how often atrial fibrillation (AF), a type of irregular heartbeat, comes back in people who have had it after a recent illness. Researchers are observing patients who already need an insertable cardiac monitor (ICM) – a small device placed under the skin to track heart rhythm – as part of their regular medical care. Specifically, they are using the Boston Scientific LUX-DX™ ICM. The main goal is to see how long it takes for AF to return within 12 months. You might be able to join if you are 18 or older, have had acute AF, and are scheduled to get or have already received a Boston Scientific LUX-DX™ ICM for clinical reasons. The study is currently unclear on its recruitment status and plans to include 100 participants.

Study design
This is an observational study, meaning researchers will watch and collect information without giving any specific treatments. It plans to enroll 100 participants.
What's involved
Not specified in the trial record.
Compensation
Not stated in the trial record.
Follow-up
Participants will be followed to see if atrial fibrillation returns within 12 months.

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NCT07434674

Incidence of Long-TeRm Atrial Fibrillation After Acute Illness

Recruiting
Not specifiedAges 18+Observational
University of California, San Diego
~100 participants
Updated 2026-02-25 on ClinicalTrials.gov

At a glance

Recruiting sites
1 of 1 listed site is recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Time to first documented event of AF by 12 months
Measured over 12 months
Atrial Fibrillation (AF)

NCT07434674

Where you'd take part

This study runs at 1 site. They're the same protocol — you choose where, and that choice sets who your contact draft is addressed to.

  • Sulpizio Cardiovascular Center

    La Jolla, Californiano site contact published

    Recruiting

Sites open and close at different times, so the status above is per site — it can differ from the study's overall status.

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Eligibility criteria

Inclusion

12-lead ECG for AF detection
24-h ECG or telemetry monitoring for AF detection and PAC analysis 4. Patient or legally authorized representative signs and dates the patient consent form. 5. Patient is ≥18 years old. 6. Patient is willing and able to comply with all study procedures and attend the required follow-up visits for the duration of the study.
  • Time to first documented event of AF by 12 months12 months

    The primary objective is to determine the time to first documented event of AF by 12 months of continuous rhythm monitoring, stratified by the setting of acute AF diagnosis (cardiac surgery, non-cardiac surgery, and medical illness).