Found 12 Stent trials
A listing of Stent medical research trials actively recruiting patient volunteers. Search for closest city to find more detailed information on a research study in your area.
The PK Papyrus Covered Coronary Stent System (PK Papyrus) received approval under a Humanitarian Device Exemption (HDE H170004) from the Food and Drug Administration on September 14, 2018 and is only indicated for treatment of acute perforations of native coronary arteries and coronary bypass grafts in vessels 2.5 to 5.0 …
This post-approval study (PAS) evaluates real world usage of the ENROUTE Transcarotid Stent when used with the ENROUTE Transcarotid Neuroprotection System in patients at standard risk for adverse events from carotid endarterectomy (a procedure to treat carotid artery disease). The study will enroll up to 400 patients at 30-60 sites …
This study will assess the feasibility and safety and to evaluate clinical outcomes of endovascular repair of complex aortic aneurysms (thoracoabdominal aortic aneurysms and aortic arch aneurysms or TAAA) in patients at high risk for open surgery in two study arms. Participants that choose to sign the informed consent and …
This study is a prospective, multicenter, single-arm study to achieve venous stent patency in the treatment of in-stent thrombosis. The study will collect data on demographics, comorbidities, details from the in-stent thrombosis diagnosis and treatment, and clinical outcomes through the 1-year follow up visit.
Normal 0 false false false EN-US JA X-NONE Patients with thoracoabdominal or pararenal aneurysm disease will be asked to take part in this research study This research study will look at treating thoracoabdominal or pararenal aneurysm disease with a new stent-graft design. The reason we are doing this research study …
This post-approval study will collect safety, performance, effectiveness, and neck dilatation data on Alto Abdominal Stent Graft System for the endovascular treatment of infrarenal abdominal aortic aneurysms and evaluate real-world outcomes in comparison to commercially available comparator devices. Penn Medicine patients with the Alto Abdominal Stent Graft System, a device …
Prospective, nonrandomized, multicenter clinical investigation of the NEXUS Aortic Arch Stent Graft System (NEXUS) for the treatment of thoracic aortic lesions involving the aortic arch with a proximal landing zone, native or previously implanted surgical graft, in the ascending aorta and with a brachiocephalic trunk native landing zone.
This is a prospective, international, multicenter, non-randomized clinical study to evaluate the safety and effectiveness of the Zenith Fenestrated+ Endovascular Graft (ZFEN+) in combination with the BeGraft Balloon-Expandable FEVAR Bridging Stent Graft System (BeGraft) for the treatment of patients with aortic aneurysms, where the device sealing zone requires fenestrations with …
Compare the safety and efficacy of the Bare Temporary Spur Stent System in subjects with infrapopliteal critical limb ischemia (CLI) to a pre-defined performance goal based on standard percutaneous transluminal balloon angioplasty (PTA). Population: infrapopliteal CLI, Rutherford class 4-5, not considered amenable to conservative medical therapy and require endovascular intervention …
Assess the safety and effectiveness of the ASG (Ascending Stent Graft) device in the treatment of lesions involving the ascending aorta and aortic arch. This study involves patients considered to be at high-risk for open surgical repair who present with the following pathologies of the ascending aorta and aortic arch …
1 - 10 of 12
- 1
- 2
