Implanted Loop Recorders for Detection and Management of Arrhythmia With Bruton Tyrosine Kinase Inhibitors

This study will enroll patients initiating Bruton Tyrosine Kinase (BTK) inhibitors without history of documented arrhythmia while on therapy using the Medtronic LINQ-2 insertable cardiac monitor (ILR). The incidence of new onset atrial fibrillation (AF) and other arrhythmia will be determined. Actions taken in response to device detected arrhythmia will be recorded.

Trial Details

NCT ID
NCT05643235
Phase
NA
Sponsor
Northwell Health
Status
RECRUITING
Cancer Type
Leukemia
Interventions
  • Medtronic LINQ-2 Insertable Cardiac Monitor (ILR)
Locations (sample)
  • New Hyde Park, New York, United States|40.7351,-73.68791

Key Eligibility Criteria

  • Willing to sign and date consent form,
  • Willing to be remotely monitored
  • Initiating BTK inhibitor for approved condition (i.e. CLL, Waldenstrom's, etc)
  • Willing to have Medtronic cardiac monitor inserted to allow at minimum 24 hours continuous monitoring prior to initiating BTK inhibitor

For full eligibility, visit ClinicalTrials.gov.

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