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Device
The Neovasc Reducer™ System for Nephrotic Syndrome (Reducer Trial)
N/A
Waitlist Available
Research Sponsored by Amir Lerman
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up baseline, 4 months post reducer implantation
Awards & highlights
Reducer Trial Summary
This trial is testing a new implantable device to see if it can improve symptoms and quality of life for patients with coronary microvascular dysfunction.
Reducer Trial Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ baseline, 4 months post reducer implantation
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~baseline, 4 months post reducer implantation
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Change in Coronary Flow Reserve (CFR)
Change in Index of Myocardial Resistance (IMR)
Reducer Trial Design
1Treatment groups
Experimental Treatment
Group I: Chronic Refractory AnginaExperimental Treatment1 Intervention
Subjects with chronic refractory angina will undergo implantation of the Neovasc Reducer™ System in the cardiac catheterization laboratory.
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
The Neovasc Reducer™ System
2021
N/A
~30
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Who is running the clinical trial?
Amir LermanLead Sponsor
Frequently Asked Questions
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