ABRE Clinical Study of the Abre Venous Self-expanding Stent System

Completed · Not applicable

Conditions studied: Iliofemoral Venous Obstruction

In brief

Evaluate the safety and effectiveness of the Abre venous self-expanding stent system for treatment of symptomatic iliofemoral venous outflow obstruction in patients with venous occlusive disease.

Key facts

Study ID

NCT03038438

Run by

Medtronic Endovascular

People needed

260

Starts

2017-12-13

Expected to finish

2022-01-28

Last updated by the study team

2022-11-08

Who can join

Age: 18 and older, up to 80. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Patient is ≥ 18 and ≤ 80 years of age;
• Patient has at least one of the following clinical manifestations (i.e. symptoms and/or signs) of venous disease in lower extremity:
• CEAP score ≥ 3
• Venous Clinical Severity Score pain score (VCSS) ≥2
• Suspected deep vein thrombosis (DVT);
• Patient is willing and capable of complying with specified follow-up evaluations at the specified times;
• Patient has been informed of the nature of the study, agrees to its provisions and has provided written informed consent, approved by the appropriate Ethics Board.
• Patient has diagnosis of non-malignant venous obstruction within the common iliac, external iliac, and/or common femoral vein. The proximal point of the obstruction may extend to the iliac venous confluence of the inferior vena cava and the distal point may be at or above the deep femoral vein. Diagnosis must be made based on objective imaging by using venography and/or intravascular ultrasound (IVUS);
• Patient has an obstructive lesion defined as:
• Occluded, or
• ≥50% in diameter reduction on venography or IVUS, or
• ≥50% area reduction on IVUS
• Acute DVT patients should be treated with the Abre stent within 14 days after onset of symptoms. Patients with acute DVT must first undergo successful treatment of acute thrombus by catheter based techniques; successful treatment is defined as 30% or less residual thrombus by venogram, as determined by physician, no bleeding, no symptomatic pulmonary embolism (confirmed by imaging), and no renal compromise (renal compromise defined as GFR>30). Patients with underlying obstructive lesions can then be included in the study within the same procedure;
• Target vessel can accommodate a 9 French Sheath, from insertion site to target segment;
• Exchangeable guidewire must cross target lesion(s) with successful predilation.

You may not qualify if…

• Patient with DVT in the target limb of which the onset of symptoms is between 15 days and 6 months prior to planned treatment or patient has an acute DVT anywhere else than in the target vessel;
• Patient has peripheral arterial disease causing symptoms in target limb;
• Patient is pregnant, female patients of child-bearing potential must have a negative pregnancy test done within 7 days prior to the index procedure;
• Patient has a known or suspected systemic infection at the time of the index procedure;
• Patient has a planned percutaneous or surgical intervention within 30 days prior or 30 days following index procedure, or a contralateral iliofemoral lesion requiring planned treatment within 12 months;
• Patient requires femoral endovenectomy and patch venoplasty, greater saphenous vein ablation, and/or small saphenous vein stripping during the index procedure;
• Patient has an active vasculitic inflammatory disorder (e.g. Behcet disease) predisposing the patient to thrombosis and requiring systemic corticosteroid therapy;
• Patient has impaired renal function (GFR < 30) or is on dialysis;
• Patient has a platelet count < 50,000 cells/mm3 or > 1,000,000 cells/mm3 and/or a White Blood Cell count < 3,000 cells/mm3 or > 12,500 cells/mm3;
• Patient has a history of bleeding diathesis or either a history or presence of heparin induced thrombocytopenia antibodies;
• Patient has a known hypersensitivity or contraindication to antiplatelets or anticoagulation, nitinol, or a contrast sensitivity that cannot be adequately pre-medicated;
• Patient has presence of other severe co-morbid conditions, which in the investigator's opinion may interfere with the patient's compliance with study visits and procedures, or may confound interpretation of study data (e.g. congestive heart failure Class III and IV, non-ambulatory patients, severe hepatic dysfunction, life expectancy < 1 year);
• Patient belongs to a vulnerable population per investigator's judgment or patient has any kind of disorder that compromises his/her ability to give written informed consent and/or to comply with study procedures. Patient must be able to consent for themselves;
• Patient is currently participating in another investigational drug or device study or observational competitive study.
• Patient has a vena cava obstruction or lesion extending into the inferior vena cava (IVC), or the presence of bilateral iliofemoral venous lesions requiring planned treatment within 12 months;
• Patient has significant venous bleeding, arterial dissection or other injury requiring additional percutaneous or surgical intervention prior to enrollment;
• Patient has a previously placed stent in the ipsilateral venous vasculature;
• Patient has disease that precludes safe advancement of the venous stent to the target lesion(s)

Where it is running

• St. Joseph Hospital — Orange, California, United States
• The Vascular Experts — Darien, Connecticut, United States
• Piedmont Atlanta Hospital — Atlanta, Georgia, United States
• University of Michigan Health System — Ann Arbor, Michigan, United States
• Mayo Clinic — Rochester, Minnesota, United States
• Holy Name Medical Center — Teaneck, New Jersey, United States
• Albany Medical Center — Albany, New York, United States
• NYU Langone Medical Center — New York, New York, United States
• The Mount Sinai Health System — New York, New York, United States
• Stony Brook Medicine — Stony Brook, New York, United States
• Carolinas Medical Center — Charlotte, North Carolina, United States
• NC Heart and Vascular Research — Raleigh, North Carolina, United States
• OhioHealth Research Institute — Columbus, Ohio, United States
• Cardiac Center of Texas — McKinney, Texas, United States
• Sentara Vascular Specialists — Norfolk, Virginia, United States
• Lake Washington Vascular, PLLC — Bellevue, Washington, United States
• Assistance Publique - Hôpitaux de Marseille - Hôpital Nord — Marseille, France
• Hôpital Européen Georges Pompidou — Paris, France
• Universitätsklinikum Aachen — Aachen, Germany
• Klinikum Arnsberg, Karolinen Hospital — Arnsberg, Germany
• Galway University Hospitals - University Hospital Galway — Galway, Ireland
• Hesperia Hospital — Modena, Italy
• University College London Hospitals NHS Foundation Trust - University College London Hospitals — London, United Kingdom
• Guy's & St Thomas' NHS Foundation Trust - St Thomas' Hospital — London, United Kingdom

Full record on ClinicalTrials.gov

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