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Active, not recruiting Not applicable

The Nordic Baltic Chronic Total Occlusion (CTO) Arrhythmia Study

NCT04542460 · tracked via the Priya Life Science Denmark tracker
Sponsor
Leif Thuesen
Phase
Not applicable
Started
2020-11-01
Last updated
2026-03-20

Condition(s) studied

Chronic Total Coronary Occlusion

Investigational drug(s) / intervention(s)

PCI

PCI: A loop recorder is implanted i all patients in both study groups to investigate: * Prevalence and severity of cardiac arrhythmias. * Effect on detected arrhythmia, in particular ventricular tachyarrhythmia, of optimal medical therapy vs. coronary revascularization by PCI. * Prevalence and severity of cardiac arrhythmias in CTO-patients with failed PCI. * Indication for prophylactic ICD implantation in CTO-patients treated conservatively or by PCI and after failed PCI. * Relation of arrhythmias to angina pectoris symptoms (CCS class), Quality of life questionnaire results and presence of myocardial reversible perfusion defects by CMRI.

Study summary

In patients with a chronic total coronary occlusion (CTO ), clinically significant arrhythmia seems to be an important and a poorly investigated problem. The arrhythmia prevalence in an all-comer CTO-population is unknown, but in ICD-populations with ischemic heart disease, a CTO may be found in half of patients with life-threatening arrhythmia.The purpose of the CTO-ARRHYTHMIA study, is to investigate the incidence of clinically significant arrhythmias in CTO patients using an implantable loop recorder. Further, the investigators intend to identify predictors for arrhythmias as well as the impact on arrhythmia of optimized pharmacological treatment and revascularization in CTO patients.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * ≥1 CTO lesion amenable to PCI. * Stable or stabilized coronary artery disease. * Angiographic/echocardiographic signs of reversible perfusion. * CTO lesion in a coronary vessel supplying a significant myocardial territory (vessel diameter usually ≥3mm). Exclusion Criteria: * Expected survival \<1 year. * Patients with an indication of ICD due to EF \< 35 or previous ventricular tachycardia. * Patients with a cardiac device i.e. ICD, pacemaker or cardiac resynchronizing treatment device. * Renal failure on dialysis. * Lesions treated with PCI within one month. * Indication for coronary artery bypass grafting (CABG). I.e. Two-or three vessel disease or left main disease and a syntax score \>22. * Significant valvular heart disease. * Declined informed consent. * Regarding CMRI: allergy to contrast medium, severe obesity, claustrophobia and certain metallic implants.

Primary outcome measure(s)

  • Rate of clinically significant arrhythmias — 1 year
    Rate og clinically significant arrhythmias in PCI versus medically only treated patients by loop recorder (table 1) and in patients with failed PCI.

Trial sites (1)

FacilityCityRegionStatus
Aalborg university hospital Aalborg North Denmark
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT04542460 on ClinicalTrials.gov ↗ ← All trials in Denmark