Prospective, Multicenter, Investigation of the Adagio Cryoablation System in Subjects With Atrial Flutter

Adagio Medical

Status

Completed

Conditions

Atrial Flutter

Treatments

Device: PolarStart System

Study type

Interventional

Funder types

Industry

Identifiers

NCT02355106

CS-001

Details and patient eligibility

About

The objective of the study is to demonstrate the safety and feasibility of the Adagio System in subjects with Atrial Flutter.

Enrollment

17 patients

Sex

All

Ages

18 to 75 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Two symptomatic episodes of typical AFl (or chronic atrial flutter) during the one-year period prior to enrollment. This may include typical AFl occurring while receiving anti-arrhythmic drug (AAD) therapy for non-AFl tachyarrhythmia, including atrial fibrillation (AF).
At least one episode of typical (clockwise or counterclockwise) atrial flutter documented by 12 lead electrocardiogram (ECG) within 6 months prior to enrollment.
Subject has been diagnosed with symptomatic AFl
Subject is at least 18 and ≤75 years of age.
Subject is able and willing to give informed consent

Exclusion criteria

Intra-cardiac thrombus has not been eliminated in subjects exposed to less than 4 weeks of therapeutic anticoagulation and a TEE (trans-esophageal echocardiogram) and/or CT did not conclusively rule out thrombus
Subject developed persistent AF at least once in history (electrical or pharmacological cardioversion after 48h or episode duration >7 days).

Subject had any previous left atrial ablation.

Subject had any previous cardiac surgery, e.g. prosthetic valves, except in the case of an isolated coronary bypass surgery performed more than three months prior to the procedure.
Subject has permanent pacemaker or defibrillator implant.
Subject has 2° type II, 3° degree atrioventricular (AV) block or left/right bundle branch block pattern
Subject has unstable angina pectoris.
Subject has history of previous myocardial infarction (MI) or percutaneous intervention during the last three months or planned in the next 3 months.

Subject has symptomatic carotid stenosis.

Subject has chronic obstructive pulmonary disease with detected pulmonary hypertension or any other evidence of significant lung disease.
Subject has any contraindication for oral anticoagulation.
Subject has any history of previous transient ischemic attack (TIA) or stroke.
Subject has known intra-cardiac thrombus formation.
Subject has any significant congenital heart defect corrected or not (except for patent foramen ovale that is allowed).
Subject has evidence of congestive heart failure (NYHA class II, III or IV) in sinus rhythm.
Subject has hypertrophic cardiomyopathy.
Subject has abnormal long or short QT interval, signs of Brugada syndrome, known inheriting ion channel disease on the family, arrhythmogenic right ventricular dysplasia.
Subject has sarcoidosis.
Subject has myxoma.
Subject has thrombocytosis (platelet count > 600,000 / μl) or thrombocytopenia (platelet count <100,000 / μl).
Subject has any untreated or uncontrolled hyperthyroidism or hypothyroidism.
Subject has renal dysfunction with glomerular filtration rate < 60 ml/min/1.72m2.
Subject has a reversible causes for AF like alcoholism.
Subject is a pregnant woman or woman of childbearing potential not on adequate birth control: only woman with a highly effective method of contraception [oral contraception or intra-uterine device] (who must have a negative pregnancy test within 1 week of randomization) or sterile woman can be enrolled.
Subject is a breastfeeding woman.
Subject has an active systemic infection.
Subject is unwilling or unable to comply fully with study procedures and follow-up due to any disease condition, which can raise doubt about compliance and influencing the study outcome especially any kind of cancer requiring ongoing in-hospital treatment, severe bleeding in history or a suspected pro-coagulant state.
Legal incapacity or evidence that a subject cannot understand the purpose and risks of the study or inability to comply fully with study procedures and follow up.
Subject has a life expectancy of ≤ 1 year.
Subject is participating in any other clinical study