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Clinical Trial Summary

The ContraBand™ device is intended for treatment of heart failure patients who remain symptomatic despite the use of optimally tolerated guideline directed medical therapy. ContraBand™ is a transcatheter constriction device which is implanted in the left and right branch pulmonary arteries, causing a local reduction in the internal diameters of these arteries, and resulting in an elevation in systolic right ventricular pressure. This may result in repositioning the interventricular septum to a more normal anatomical position, and supporting it with a "counter-pressure" during systole of the left ventricle. This study is a first-in-human, early feasibility, multi center, prospective, interventional, open-label, single-arm study.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05230745
Study type Interventional
Source Restore Medical Ltd
Contact Stephen Bellomo
Phone +972 54 227 4831
Email stephen@restoremedical.co
Status Recruiting
Phase N/A
Start date October 7, 2021
Completion date December 31, 2026

See also
  Status Clinical Trial Phase
Terminated NCT03774615 - ORal IrON Supplementation With Ferric Maltol in Patients With Heart Failure Carrying Left Ventricular Assist Devices Phase 4
Active, not recruiting NCT05350969 - Study to Assess Efficacy and Safety of CDR132L in Patients With Reduced Left Ventricular Ejection Fraction After Myocardial Infarction Phase 2
Terminated NCT03148847 - Management of Cardiogenic Pulmonary Edema (RENAU-OAP)
Completed NCT04397302 - Role of Sacubitril/Valsartan in the Improvement of Heart Failure With Reduced Ejection Fraction