Venous Insufficiency of Leg
Conditions
Brief summary
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.
Interventions
DEVICECook® Venous Valve System
The Cook® Venous Valve is a permanent prosthetic, bicuspid, one-way flow valve designed to be percutaneously implanted into the peripheral deep venous system. The Cook® Venous Valve Delivery System is used to percutaneously deliver the Cook® Venous Valve into the deep venous system.
Sponsors
MED Institute Inc.
Study design
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion 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
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Freedom from major adverse events in the first 30 days | 30 days after enrollment | The primary safety endpoint is freedom from major adverse events (MAE) in the first 30 days, where MAE is defined as: death, clinically-driven reintervention, bleeding requiring transfusion, flow limiting dissection of the target vessel, or clinically significant deep vein thrombosis (DVT), pulmonary embolism, or device migration. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Freedom from MAE at three months, six months, and 12 months | Three months, six months, and 12 months after enrollment | The secondary safety endpoint is freedom from MAE at three months, six months, and 12 months. |
Countries
Colombia
Outcome results
None listed