The GORE® VIAFORT Vascular Stent Iliofemoral Study

W.L. Gore & Associates

Status

Enrolling

Conditions

Venous Leg Ulcer

Venous Ulcer

Vein Thrombosis

Venous Occlusion

Vein Occlusion

Vein Disease

Venous Stasis

Venous Disease

Venous Stenosis

Venous Thromboses

Treatments

Device: GORE® VIAFORT Vascular Stent

Study type

Interventional

Funder types

Industry

Identifiers

NCT05489588

VNS 21-07

Details and patient eligibility

About

This study is a prospective, non-randomized, multicenter, single-arm, clinical study to evaluate the performance, safety and efficacy of the GORE® VIAFORT Vascular Stent for treatment of symptomatic iliofemoral venous obstruction.

Full description

A maximum of 30 clinical sites across the U.S. will participate in the study. One hundred and sixty-five subjects are intended to be implanted with the GORE® VIAFORT Vascular Stent in this study, with a limit of 33 treated subjects per site. Subjects will be evaluated through hospital discharge and return for follow-up visits at 1, 6, 12, 24, 36, 48, and 60 months post-treatment.

Enrollment

165 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

Preoperative Inclusion Criteria:

Patient is at least 18 years of age.
Patient is willing and able to comply with all follow-up evaluations as well as any required medication or compression regimen.
Patient is able to provide informed consent.
One of the following: Clinical severity class of CEAP 'C' classification ≥3 or rVCSS pain score ≥2.
Intention to treat the target areas with only the GORE® VIAFORT Vascular Stent.
Estimated life expectancy ≥1 year.
Patient is ambulatory (use of assistive walking device such as a cane or walker is acceptable).
Patient has adequate inflow to the target lesion(s), per investigator/sub-investigator discretion, involving at least a patent femoral or deep femoral vein.
Presence of non-malignant symptomatic unilateral iliofemoral venous obstruction.

Preoperative Exclusion Criteria:

Patient has DVT in the target areas with symptom onset date greater than 14 days but less than or equal to 90 days prior to treatment.
Patient is a pregnant or breastfeeding woman, or a woman planning to become pregnant through the 12-month visit.
Patient has clinically significant (e.g., symptoms of chest pain, hemoptysis, dyspnea, hypoxia, etc.) pulmonary embolism (confirmed via Computed Tomography Angiography) at the time of enrollment.
Patient has a known uncorrectable bleeding diathesis or active coagulopathy meeting the following definitions (all must be tested for):
1. uncorrected INR>2 (not as a result of warfarin or DOAC therapy), OR
2. platelet count <50,000 or >1,000,000 cells/mm3, OR
3. white blood cell count <3,000 or >12,500 cells/mm3
Patient has impaired renal function (eGFR <30 mL/min/1.73m2) or is currently on dialysis.
Patient has uncorrected hemoglobin of <9 g/dL.
Patient has known history of antiphospholipid syndrome (APS).
Patient has known homozygous or acquired coagulation defect (e.g., Protein C or Protein S deficiency) that cannot be treated with therapeutic anticoagulation.
Patient has a planned surgical intervention that has the potential to clinically interfere with the endpoints of this treatment (other than pre-stenting procedures such as thrombolysis or thrombectomy) within 30 days prior to or within 30 days after the planned study procedure. Examples include surgical interventions that may impact mobility, and surgical interventions that require cessation of therapeutic antiplatelet or anticoagulation within 30 days following the index procedure.
Patient has had or requires open deep venous surgery in the target limb.
Patient is currently participating in another investigational drug or device study that has not completed the primary endpoint or that clinically interferes with the endpoints of this treatment, in the opinion of the investigator/sub-investigator. Observational studies are permitted.
Patient has had a previous major (i.e., above the ankle) amputation of the target lower limb.
Patient has known sensitivity to device materials.
Patient has had prior stenting or grafts in the target vessels.
Patient has a known or suspected active systemic infection at the time of the index procedure. Patients with a chronic infection (e.g., HIV, hepatitis C) that can be managed, and with an active clinical plan in place may be eligible.
Patient has known history of intravenous drug abuse within one year of treatment.
Patient has significant peripheral arterial disease (chronic Rutherford Type 2 or greater, acute Rutherford Type IIa or greater).
Patient has a BMI >45. Patients with a BMI of up to 45 may be enrolled provided that diagnostic quality ultrasound of the implant sites can be performed.
Patient is actively undergoing or plans to begin cancer treatment.
Patients with hypercoagulable states that are unwilling to take anticoagulant medications on a long-term basis.
Patient has contraindication to thrombolytics, anticoagulants, or iodinated contrast necessary for the index procedure and long-term medical therapy (contrast pre-medication is acceptable).

Intraoperative Inclusion Criteria:

Presence of non-malignant unilateral obstruction of the common femoral vein, external iliac vein, and/or common iliac vein defined as occlusion or at least 50% reduction in target vessel lumen as measured by procedural IVUS and venogram.
Patient can accommodate an appropriately sized GORE® VIAFORT Vascular Stent as per reference vessel diameter (see IFU), as determined by intraoperative IVUS post pre-dilation.
Patient must have appropriate access vessels to accommodate the delivery sheath for the selected device size.
Patient has adequate landing zones free from significant disease requiring treatment within the native vessels beyond the proximal and distal margins of the lesion.
Patient has adequate inflow to the target lesion(s), per investigator/sub-investigator discretion, involving at least a patent femoral or deep femoral vein.
Lesion can be traversed with a guidewire.
Disease involves only unilateral iliofemoral venous segments with intent to stent all affected iliofemoral segments. Patients with disease extending into the inferior vena cava or contra-lateral iliofemoral veins who are anticipated to require endovascular or surgical treatment within 12 months after investigational device implant will be excluded.
Patient does not have significant (i.e., >20% residual thrombosis) acute thrombus within the target stent area at the time of investigational device placement. Patients with acute thrombus within the target stent area must have thrombus successfully treated prior to investigational device placement. Successful thrombus treatment is defined as reestablishment of antegrade flow with ≤20% residual thrombosis as confirmed by IVUS and venogram, AND freedom from bleeding, vascular injury, or hemodynamically significant pulmonary embolism. After successful thrombus treatment, investigational device placement can occur within the same procedure.