The Nordic Baltic Chronic Total Occlusion (CTO) Arrhythmia Study
Primary Purpose
Chronic Total Coronary Occlusion
Status
Recruiting
Phase
Not Applicable
Locations
Denmark
Study Type
Interventional
Intervention
PCI
Sponsored by
About this trial
This is an interventional basic science trial for Chronic Total Coronary Occlusion
Eligibility Criteria
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.
Sites / Locations
- Aalborg university hospitalRecruiting
Arms of the Study
Arm 1
Arm 2
Arm Type
No Intervention
Active Comparator
Arm Label
Optimal Medical Treatment
Optimal Medical Treatment and PCI
Arm Description
CTO patients receiving optimal medical treatment
CTO patients receiving PCI in ajunction to optimal medical treatment
Outcomes
Primary Outcome Measures
Rate of clinically significant arrhythmias
Rate og clinically significant arrhythmias in PCI versus medically only treated patients by loop recorder (table 1) and in patients with failed PCI.
Secondary Outcome Measures
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT04542460
Brief Title
The Nordic Baltic Chronic Total Occlusion (CTO) Arrhythmia Study
Official Title
Chronic Total Coronary Occlusion; Arrhythmia in Patients With Adjunction of PCI to Optimal Medical Treatment Versus Optimal Medical Treatment and in Patients With Failed PCI.
Study Type
Interventional
2. Study Status
Record Verification Date
February 2023
Overall Recruitment Status
Recruiting
Study Start Date
November 1, 2020 (Actual)
Primary Completion Date
March 1, 2024 (Anticipated)
Study Completion Date
September 1, 2027 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Leif Thuesen
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes
5. Study Description
Brief 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.
Detailed Description
In angiographic materials, chronic total coronary occlusion (CTO) is present in approximately 15-25% of patients and in 25-50% of those with significant coronary disease. Until recently, because of low procedural success and increased risk of complications, PCI was a problematic treatment in these patients. The introduction of drug eluting stents and a variety of dedicated CTO devices combined with the evolution of specific CTO techniques have made revascularization by PCI a promising treatment.
In CTO patients, 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. Further, in patients with ischemic heart disease receiving ICDs as primary prevention, presence of a CTO was an independent predictor of occurrence of ventricular arrhythmias, and in survivors of out-of-hospital cardiac arrest, the risk of ventricular arrhythmias was found to be increased in patients with a chronic total coronary occlusion. Nevertheless, the genesis of arrhythmia in CTO-patients is likely to be multifactorial. It has been documented, that ischemic heart disease patients who present with a chronic occlusion of at least one coronary artery are older and have additional risk factors such as hypertension, diabetes, lower left ventricular ejection fraction (LVEF) and more frequent myocardial infarction, i.e. a higher Chads2Vasc score (risk score for stroke in atrial fibrillation patients). Although LVEF is lower in patients with a chronic coronary occlusion, less than 1/3 are potential ICD candidates with an LVEF <35%. However, a recent study in consecutive post-AMI survivors documented the highest incidence of sudden cardiac death in patients with a relatively preserved LVEF.
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 investogators intend to identify predictors for arrhythmias as well as the impact on arrhythmia of optimized pharmacological treatment and revascularization in CTO patients. Here, CTO patients with failed PCI may be individuals with a particularly high risk of severe arrhythmias.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Chronic Total Coronary Occlusion
7. Study Design
Primary Purpose
Basic Science
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Investigator conceived, initiated and driven 1:1 randomized open label clinical trial
Masking
None (Open Label)
Allocation
Randomized
Enrollment
200 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Optimal Medical Treatment
Arm Type
No Intervention
Arm Description
CTO patients receiving optimal medical treatment
Arm Title
Optimal Medical Treatment and PCI
Arm Type
Active Comparator
Arm Description
CTO patients receiving PCI in ajunction to optimal medical treatment
Intervention Type
Procedure
Intervention Name(s)
PCI
Other Intervention Name(s)
Loop recorder
Intervention Description
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.
Primary Outcome Measure Information:
Title
Rate of clinically significant arrhythmias
Description
Rate og clinically significant arrhythmias in PCI versus medically only treated patients by loop recorder (table 1) and in patients with failed PCI.
Time Frame
1 year
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
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.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Leif Thuesen, DMSc
Phone
+4597664465
Email
leif.thuesen@rn.dk
First Name & Middle Initial & Last Name or Official Title & Degree
Martin K Christensen, MD
Phone
+4522759228
Email
m.kirk@rn.dk
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Peter Soegaard, DMSc
Organizational Affiliation
Co-PI
Official's Role
Study Chair
Facility Information:
Facility Name
Aalborg university hospital
City
Aalborg
State/Province
Region Nordjylland
ZIP/Postal Code
9000
Country
Denmark
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Leif Thuesen, Doctor
Phone
+4597664465
Email
leif.thuesen@rn.dk
12. IPD Sharing Statement
Plan to Share IPD
No
IPD Sharing Plan Description
Data will be analyzed at site
Learn more about this trial
The Nordic Baltic Chronic Total Occlusion (CTO) Arrhythmia Study
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