Atrial Fibrillation Trial, Recruiting
Who may be able to join
AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI
Who might be able to join this trial:
- People who already have a medical reason to have a small heart-monitoring device (called an insertable cardiac monitor) placed under their skin as part of their normal care.
- People who are scheduled to receive, or have already received, a specific heart monitor called the Boston Scientific LUX-DX™.
- People who have had an episode of atrial fibrillation (an irregular heart rhythm) that was detected in a hospital or urgent care setting, or during a serious illness, and who have had specific heart-tracing tests (a 12-lead ECG and at least 24 hours of heart monitoring) to confirm this.
- People who are 18 years of age or older.
- People who are willing and able to attend all required study visits and follow the study procedures for the full duration of the trial.
- People (or their legal representative) who have signed and dated the study consent form.
Who may not be able to join:
- People who have a known history of atrial fibrillation or a related heart rhythm problem (atrial flutter) before the episode that brought them into the study.
- People who need to take heart rhythm medications for a reason other than this recent episode of atrial fibrillation.
- People who, in their treating doctor's opinion, have a permanent medical reason that would rule out ever taking blood-thinning medication for atrial fibrillation management.
- People who are currently enrolled in another clinical trial that could affect the results of this study.
- People whose treating doctor has determined they have a life expectancy of less than one year.
- People who are pregnant.
- People who already have a medical reason to receive a different type of implanted heart device, such as a pacemaker, defibrillator, or implantable heart pressure monitor, as this could overlap with or interfere with the study device.
- People who are unable or unwilling to follow the required study procedures.
Important: Always verify eligibility with the trial site directly before applying.
Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.
Contact this trial
Phone: 858-246-2016
Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.
GP referral letter
Print a one-page summary to share with your doctor.
Trial details
Where this trial is recruiting
Primary endpoints
Time to first documented event of AF by 12 months
Can't join this trial?
Data last synced from ClinicalTrials.gov: 26 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.