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NCT05643235

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

Recruiting now NA Last updated 18 September 2025
What this trial tests

NA trial testing Medtronic LINQ-2 Insertable Cardiac Monitor (ILR) in Atrial Fibrillation in 50 participants. Currently enrolling.

Timeline
1 January 2023
Primary endpoint
1 December 2026
1 December 2030

Quick facts

Lead sponsorNorthwell Health
PhaseNA
StatusRecruiting now
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposeother
Enrollment50
Start date1 January 2023
Primary completion1 December 2026
Estimated completion1 December 2030
Sites1 location across United States

Drugs / interventions tested

Conditions studied

Sponsor

Northwell Health — full company profile →

Who can join

18 and older, any sex, with Atrial Fibrillation or Supraventricular Arrhythmia. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

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.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Atrial Fibrillation

Currently open trials in the same condition.

Other Northwell Health trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT05643235.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing