Access Safety and Efficacy Post Endovascular Intervention
This trial is active, not recruiting.
|Treatment||arstasis access system (axera)|
|Start date||December 2012|
|End date||March 2015|
|Trial size||240 participants|
|Trial identifier||NCT01773148, RC-03773|
The goal of this study is to assess the safety and effectiveness of the AXERA Access System in subjects undergoing Common Femoral Artery (CFA) access for Percutaneous Coronary Intervention (PCI) and/or Peripheral Vascular Intervention (PVI) through a 5 French (F) or 6F introducer sheath.
|United States||No locations recruiting|
|Other countries||No locations recruiting|
|Huntsville, AL||Heart Center Research, LLC||no longer recruiting|
|Little Rock, AR||Arkansas Heart Hospital||no longer recruiting|
|La Jolla, CA||Scripps Green||no longer recruiting|
|Loma Linda, CA||Loma Linda University Health||no longer recruiting|
|Sacramento, CA||Mercy Heart and Vascular Institute||no longer recruiting|
|Stockton, CA||St. Joseph's Medical Center||no longer recruiting|
|Newark, DE||Christiana Care||no longer recruiting|
|Macon, GA||Medical Center of Central Georgia||no longer recruiting|
|Opelousas, LA||Opelousas General Health System||no longer recruiting|
|Baltimore, MD||Sinai Hospital||no longer recruiting|
|Hattiesburg, MS||Hattiesburg Clinic||no longer recruiting|
|Tupelo, MS||Northern Mississippi Medical Center||no longer recruiting|
|Las Vegas, NV||St. Rose Dominican||no longer recruiting|
|Tulsa, OK||St. John Medical Center||no longer recruiting|
|Anderson, SC||AnMed Health||no longer recruiting|
|West Columbia, SC||Lexington Medical Center||no longer recruiting|
|Tacoma, WA||Franciscan Research Center||no longer recruiting|
|Endpoint classification||safety/efficacy study|
|Intervention model||single group assignment|
Placement of AXERA device in subjects undergoing common femoral artery access for PCI and/or PVI through a 5F or 6F introducer sheath.
Major Adverse Events
time frame: Procedure through 30 day follow-up.
time frame: Day 1-Day of Procedure.
Time to Hemostasis (TTH)
time frame: Immediately following procedural sheath removal.
Time to Ambulation (TTA)
time frame: Evaluated at any time after 2 hours post sheath removal, until the subject successfully ambulated.
Time to Discharge, eligibility (TTD/e)
time frame: Evaluated following sheath removal and ambulation and physical examination of the access site demonstrating stable access site.
Time to Discharge, actual (TTD/a)
time frame: Evaluated following procedural sheath removal until actual discharge.
Minor Adverse Events
time frame: Procedure through 30 day follow-up.
Male or female participants at least 18 years old.
Inclusion Criteria: - Subject is 18 years of age or older. - Subject is clinically indicated for a PCI or PVI involving access through a 5F or 6F introducer sheath in the femoral artery. - Subject is able to ambulate without assistance prior to the procedure and can be expected to ambulate (20 feet) within 2 hours post procedure. - Female subjects of child bearing potential must have a negative pregnancy test. Exclusion Criteria: - Subjects who are pregnant or lactating. - Subject has a pre-existing severe non-cardiac systemic disease/illness or another reason that results in a projected life expectancy of less than 1 year. - Subject has an active systemic or cutaneous infection or inflammation (e.g., septicemia at the time of the procedure). - Subject has systemic hypertension unresponsive to treatment (>180mmHg systolic and >110mm diastolic). - Subject has significant bleeding coagulopathy or platelet disorder, (INR> 2.0), including known thrombocytopenia (platelet count <100,000/µL), thrombasthenia, Von Willebrand's disease, Factor V deficiency, or anemia (hemoglobin <10 g/dL, or hematocrit <30%). - Subject presents with chronic renal insufficiency (creatinine ≥3.0mg/dl). - Subject presents with hemodynamic instability or is in need of emergent surgery or emergent procedure. - Subject presents with ST elevation myocardial infarction. - Subject presents with unstable angina or non-ST elevation myocardial infarction and has troponin level > 3 X upper limit of normal. There must be at least one troponin level drawn > 6 hours after onset of chest pain. - Subject has received low molecular weight heparin < 8 hours before vascular access, glycoprotein IIb/IIIa inhibitor < 24 hours before vascular access, unfractionated heparin by infusion < 1 hour before vascular access, or parenteral heparin at anticoagulant dose (as opposed to DVT prophylaxis)< 6 hours before vascular access. - Subjects who are clinically obese, defined as BMI >40. - Subject has received femoral artery Vessel Closure Implant (VCI) (suture or staple) at the target access site. - Subject has received femoral artery VCI (collagen/PEG/PGA) at the target access site within 90 days of AXERA procedure. - Subject is unable to routinely walk at least 20 feet without assistance (e.g., requires a walker or wheelchair to mobilize, is leg amputee or has known paralysis) or unable to ambulate within 2 hours post procedure. - Subject has had prior vascular surgery or vascular grafts at the target femoral artery access site. - Subject has had a previous target femoral artery complication from angiography (such as pseudoaneurysm, Arteriovenous (AV) fistula, dissection), small CFA, abnormal, absent or weak distal ipsilateral pulse, or presenting with clinically significant peripheral vascular disease in the vicinity of the puncture. - Subject has a high puncture (i.e. above the inferior reflection of the inferior epigastric artery). - Subject has antegrade puncture. - Subject has a stent in the ipsilateral common femoral artery. - Subject is currently participating in an investigational drug or another device study that clinically interferes with the current study endpoints.
|Official title||AXERA Access Safety and Efficacy Post Endovascular INtervention|
|Principal investigator||Mark Dorogy, MD|
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