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Clinical Trial Summary

The study objectives are to assess safety and effectiveness, measured acutely and at the 30-day visit after implantation of the Valiant Captivia physician fenestrated Stent Graft. Clinical utility measures throughout the procedure and until discharge will be assessed


Clinical Trial Description

Prospective, single-arm, non-randomised, multicenter, investigator initiated clinical study evaluating subjects implanted with The Valiant Captivia physician fenestrated stent graft for the treatment of aneurysms/penetrating ulcers, Type B aortic dissections or residual dissection after Type A repair, of the aortic arch and the descending thoracic aorta which are candidates for revascularisation of all three supra-aortic vessels (BT (brachiocephalic trunk) , LCCA (left Common Carotid artery), LSA (Left Subclavian Artery) ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05479305
Study type Interventional
Source Ceric Sàrl
Contact Laure Morsiani, PhD
Phone +33.1.76.73.92.36
Email contact@cerc-europe.org
Status Recruiting
Phase N/A
Start date November 21, 2023
Completion date October 2027

See also
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Not yet recruiting NCT05349071 - PreOperative Methylprednisolone on Thoracic Endovascular Repair for Reducing Post-implantation Syndrome (POMTEVAR) N/A
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Enrolling by invitation NCT03845829 - LSA Reconstruction With Laser Fenestration During the TEVAR N/A
Active, not recruiting NCT04765605 - Guo's Subclavian Artery Reconstruction: The Prospective, Multiple Center Study of WeFlow-Tbranch Stent Graft System(GUEST Study) N/A
Recruiting NCT06087029 - IMPRoving Outcomes in Vascular DisEase- Aortic Dissection N/A