Cook Venous Valve System for Treatment of Chronic Venous Insufficiency

MED Institute

Status: Active, not recruiting

Conditions: Venous Insufficiency of Leg

Treatments: Device: Cook® Venous Valve System

Study type: Interventional

Funder types: Industry

Identifiers

NCT05883943

21-4344

Details and patient eligibility

About

The purpose of this study is to learn about the safety, efficacy and utility of a medical device called the Cook® Venous Valve System. This device, percutaneously placed in the leg, is meant to help the blood flow correctly through the veins in the leg.

Enrollment: 4 patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion and exclusion criteria

Limited inclusion criteria:

• Documented symptomatic deep venous reflux in one limb
• Deep venous reflux in the region of interest

Limited exclusion criteria:

General:

• Age < 18 years
• BMI ≥ 40
• Cultural objections to porcine materials
• Unwillingness or inability to comply with the follow-up
• Unwillingness to provide study data for duration of study
• Simultaneous participation in another device or drug study
• Inability or refusal to give informed consent

Medical:

• Pregnant, or planning to become pregnant
• Diagnosis of terminal illness with life expectancy less than 12 months
• Complete symptom resolution with compliant compression therapy for three months
• Untreated superficial venous disease
• Medical interventions including any of the following: planned procedure of any leg, vascular intervention or major surgery within the last three months, implanted inferior vena cava filter
• Medical history of any of the following: anticoagulation treatment for pulmonary embolism (within the last six months or ongoing), insulin dependent diabetes, chronic obstructive pulmonary disease, renal dysfunction requiring dialysis, leg amputation, bleeding diathesis, untreated or unresolved systemic infection or local infection, active malignancy except non-melanoma skin cancer, other acute or chronic medical condition that may cause noncompliance with the protocol or confound the study results, documented history of significant untreated stenosis within the arterial system
• Positive coronavirus (COVID-19) test six days prior to implant procedure

Anatomical:

• Inability to clearly visualize target implantation site
• Tortuous target implantation site
• Inadequate inflow and/or outflow to the target region

Procedural:

• Inability to gain access to the access site vein
• Untreated focal or diffuse stenosis

Trial design

Primary purpose: Treatment

Allocation: N/A

Interventional model: Single Group Assignment

Masking: None (Open label)

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4 participants in 1 patient group

Cook® Venous Valve System

Experimental group

Treatment:

Device: Cook® Venous Valve System