VALIANT CAPTIVIA Post-market Registry

N/ATerminatedNCT01181947

Medtronic Cardiovascular100 enrolled

Overview

The Valiant Thoracic Stent Graft has been preloaded on the new Captivia Delivery System (Captivia). This new delivery system was CE marked on September 14th, 2009 and was commercially released in the European Union on October 1st, 2009. The Valiant Thoracic Stent Graft with the Captivia Delivery System (Valiant Captivia) is designed to treat diseases of the descending thoracic aorta including but not limited to aneurysms and dissections. The purpose of the VALIANT CAPTIVIA Registry is to collect and evaluate mid term clinical performance data of the Valiant Captivia Thoracic Stent Graft System following OUS market approval.

1. Use of controls 1. This study is a post-market registry without using a control. All analyses will be descriptive in nature and no statistical comparisons are planned. Sample size 2. There is no sample size calculation since this is not a hypothesis driven study; VALIANT CAPTIVIA has recruited 100 subjects and will follow these subjects through for approximately 36 months. 2. Number of investigation sites and study duration 1. 15 investigation sites in Europe and Turkey where the Valiant Captivia Thoracic Stent Graft System is commercially available have enrolled 100 subjects. 2. There will be no minimum nor maximum number of enrolled subjects per investigation site. 3. The sites' compliance with the clinical investigation plan will be assessed on an ongoing basis. In case of serious non-compliance, the sponsor may decide to stop subject enrolment in a site based on the assessment.

Study Type

OBSERVATIONAL

Enrollment

100

Conditions

Aortic Aneurysm, Thoracic

Interventions

TEVARDEVICE

Thoracic endovascular aneurysm repair

Eligibility

Sex: ALL

Medical Language ↔ Plain English

Inclusion criteria * Age ≥ 18 years or minimum age as required by local regulations * Indication for surgical repair of thoracic aortic aneurysms and/or thoracic aortic dissections with an thoracic endovascular stent graft in accordance with the applicable guidelines on endovascular interventions and the Instructions for Use of the Valiant Captivia Thoracic Stent Graft System * Signed consent form ('Patient informed consent form' or 'Patient Data Release Authorization Form') * Intention to implant the Valiant Captivia Thoracic Stent Graft System or having implanted the system within the last 3 months before subject enrollment * Willingness and ability to comply with the CIP Exclusion criteria * High probability of non-adherence to physician's follow-up requirements * Participation in concurrent interventional trial which may confound study results * Prior implantation of a thoracic stent graft

Locations (15)

Medical University of Innsbruck

Innsbruck, Austria

Klinikum der J.W.Goethe-Universitat

Frankfurt am Main, Germany

Klinikum der Johann-Wolfgang-Goethe - Institut fur Diagnostische und Interventionelle Radiologie

Outcomes

Primary Outcomes

Treatment Success

technical success and freedom from * TAA diameter increase of stented segment (\>5mm compared to 1 mo), * Types I/III endoleak, * Aneurysm rupture, * Conversion to open surgery, * Stent graft occlusion, * Stent graft migration resulting in SAE or secondary intervention.

Time frame: at 12 months

Technical Success at Time of Initial Implant

Technical success is defined as successful delivery and deployment of the stent graft (assessed intraoperatively). This is achieved by deployment of the Valiant Thoracic Stent Graft in the planned location with no unintentional coverage of the left subclavian artery, left common carotid artery and/or brachiocephalic artery and with the removal of the delivery system

Time frame: intraoperatively

Secondary Outcomes

SAE

Serious Adverse Events (SAE)

Time frame: through 12 months

ACM and ARM

All-cause (ACM), Aneurysm related (ARM) and dissection related mortality

Time frame: at 30 days, 12 months, 24 months and 36 months

Data from ClinicalTrials.gov

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