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Subcutaneous Cardiac Monitoring of Patients With BTK Inhibitors — IRAF-ISCM  

Atrial Fibrillation Clinical Trial

Official title:
Electrocardiographic Changes and Rhythm Disorders Associated With BTK Inhibitors Exposure Using an Insertable Subcutaneous Cardiac Monitor: a Multicenter Cardio-Oncology Prospective Cohort

Clinical Trial Summary

The goal of this clinical trial is to screen all types of electrocardiographic changes and rhythm disorders in adult patients with a hematologic malignancy requiring a treatment by Bruton's tyrosine kinase (BTK) inhibitor (ibrutinib, acalabrutinib, zanubrutinib) using an insertable subcutaneous cardiac monitor (ISCM) and occurring from inclusion and within 12 months. This study consists of the implantation of an ISCM at inclusion and before BTK inhibitor initiation. Then patients will have medical visits every 3 months (+/- 7 days) during 12 months and a continuous cardiac telemonitoring using the ISCM.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT06029166
Study type Interventional
Source University Hospital, Caen
Contact Joachim Alexandre, MD, PhD
Phone +33 2.31.06.46.71
Email alexandre-j@chu-caen.fr
Status Not yet recruiting
Phase N/A
Start date October 1, 2023
Completion date October 1, 2026
View Details
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