InnoVein Valve Treatment: Subjects will have the InnoVein Valve implanted
Study summary
This objective of this feasibility study is to evaluate the safety of the InnoVein Valve and Delivery System for treatment of chronic venous insufficiency.
Eligibility
Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Key Inclusion Criteria:
* Willing and able to provide written Informed Consent
* Diagnosis of symptomatic non-obstructive chronic valvular insufficiency of the femoral vein
* Willing and medically able to receive intraprocedural and post-procedural anticoagulation medication
* Life expectancy \>1yr
* Reflux time \>1s in the superficial femoral and/or popliteal vein
Key Exclusion Criteria:
* Any prior deep vein intervention within 6 months prior to the Index Procedure
* History of 2+ DVTs
* Inadequate inflow to the femoral vein or inadequate outflow through the femoral vein, iliac vein, or IVC
* Current IVC Placement
* History of pulmonary embolism within 6 months
* Conditions that increase the risk of device thrombosis or patient bleeding
* Any planned surgical or interventional procedure within 30 days prior to or after the Index Procedure
* Investigator or sponsor believes the subject would not benefit, would not be appropriate, be unable to follow-up, or be at high risk for non-compliance with the protocol
Primary outcome measure(s)
Safety of the InnoVein Valve and Delivery System: Number of Major Adverse Events — 30 Days Number of Major Adverse Events
Trial sites (3)
Facility
City
Region
Status
Hollywood Private Hospital
Nedlands
Western Australia
Recruiting
Sir Charles Gairdner Hospital
Nedlands
Western Australia
Recruiting
Flinders
Adelaide
Australia
Recruiting
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.
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