Found 43 su-surgery-administration trials
A listing of su-surgery-administration medical research trials actively recruiting patient volunteers. Search for closest city to find more detailed information on a research study in your area.
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This is a prospective, multicenter, single-blind, randomized (2:1), controlled trial to evaluates the safety and efficacy of the MAGNITUDE S-BRS in the treatment of chronic limb-threatening ischemia due to de novo or restenotic lesions in the infrapopliteal arteries compared to standard PTA alone.
The study will be a prospective, multi-center, non-randomized trial with all subjects enrolling into a single arm receiving the inQB8 MonarQ TTVR system. Subjects suffering from severe or greater, symptomatic tricuspid regurgitation who are anatomically suitable for the MonarQ device and who have been determined to be intermediate or high …
Prospective, multicenter, non-randomized, single-arm study with a primary and secondary arm. The purpose of the study is to assess the safety and effectiveness of the ASG device in the treatment of de novo Type A aortic dissections. Please reference Sections 2 and 3 for further information.
Patients with renal insufficiency who undergo cardiac surgery with cardiopulmonary bypass are at significant risk for exacerbation of renal dysfunction postoperatively. The JuxtaFlow Renal Assist Device is designed to sustain or enhance glomerular filtration perioperatively for patients with renal insufficiency by applying a mild controlled negative pressure to the collecting …
This research study will evaluate changes in chin volume following treatment with an FDA-approved hyaluronic acid filler (Restylane Lyft) manufactured by Galderma that is used as part of standard care for chin augmentation. The primary goal of the study is to measure how chin volume changes over time after filler …
Clinical data from this study will support the intended use of the Rapidlink device, a vascular prosthesis for replacement or bypass of diseased vessels in patients with aneurysmal or other vascular diseases. It is indicated for repair or replacement of aortic branch vessels during open aortic arch repair. Rapidlink simplifies …
In two patients with severe liver disease, we used a novel support system, extracorporeal liver cross-circulation (ELC), that temporarily connects the patients blood circulation to a donor liver outside the body. Both treatments lasted 1319 hours and were completed without serious complications. The procedures were stopped early due to clotting …
This study investigates the use of image-guided surgery with indocyanine green for imaging solid tumors. The purpose is to evaluate the safety and effectiveness of this method compared to the standard surgical care. Patients involved are those with solid tumors or diseased tissue, including benign nodules, which are considered resectable …
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 …
The purpose of DT PAS PSR is to -Provide continuing evaluation and periodic reporting of safety and effectiveness of Medtronic market-released products for their intended use -To further confirm safety and effectiveness of the HVAD System when used as intended for DT, in real-world clinical practice The purpose of Apogee …
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