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Clinical Trials/NCT02800837
NCT02800837
Unknown
Not Applicable

Multicenter Prospective Clinical Study of the STENTYS Xposition S for Treatment of Unprotected Left Main Coronary Artery Disease

Stentys4 sites in 3 countries200 target enrollmentMay 2016

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Coronary Artery Disease (Left Main)
Sponsor
Stentys
Enrollment
200
Locations
4
Primary Endpoint
Efficacy Endpoint - Angiographic Success
Last Updated
9 years ago

Overview

Brief Summary

Prospective, non-randomized, multi-center study assessing the long term safety and efficacy of the self expandable sirolimus eluting Xposition S stent in the treatment of unprotected left main coronary artery disease.

Detailed Description

In the treatment of unprotected left main coronary artery (ULMCA) disease, previous mono-center studies have shown promising results with the previous generation of the self-expandable STENTYS stent (paclitaxel eluting stent, delivered via withdrawal of a sheath). The TRUNC study aims at assessing at large scale the Xposition S in the treatment of ULMCA disease. The Xposition S is a sirolimus eluting stent, mounted on a balloon delivery system. The study aims at collecting clinical practice routine data from 200 patients.

Registry
clinicaltrials.gov
Start Date
May 2016
End Date
June 2019
Last Updated
9 years ago
Study Type
Observational
Sex
All

Investigators

Sponsor
Stentys
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Subject ≥ 18 years old;
  • Presence of coronary artery stenosis in the unprotected Left Main (LM) Coronary Artery which is indicated for PCI and Xposition S stent treatment
  • Left Main Coronary Artery reference vessel diameter ranging from 2.5 mm to 6.0 mm;
  • The subject is able to provide voluntary informed consent, willing to comply with all study requirements and sign the written informed consent.

Exclusion Criteria

  • Recent STEMI (\<1 month) ;
  • SYNTAX score ≥ 33 ;
  • Highly calcified lesions or excessive tortuosity at target lesion site;
  • Subject unable to comply with dual antiplatelet therapy as recommended per guidelines;
  • Planned cardiac surgery or valve intervention within the next 12 months.
  • Participation to other investigational drug or device studies that have not reached their primary endpoint.

Outcomes

Primary Outcomes

Efficacy Endpoint - Angiographic Success

Time Frame: 12 months post-procedure

Achievement of \<20% final residual stenosis at target lesion (visual estimation) with TIMI 3 flow in main branch

Clinical Endpoint- Target Lesion Failure (TLF)

Time Frame: 12 months post-procedure

TLF defined as cardiac death, MI not attributable to a non target vessel, or clinically driven target lesion revascularization

Secondary Outcomes

  • Procedural Success(48 hours post procedure (hospital discharge))
  • Clinically Driven Target Lesion Revascularization(30 days, 12 months and 24 months post procedure)
  • MI rate (not attributable to a non target vessel)(30 days, 12 months and 24 months post procedure)
  • Stroke Events Rate(30 days, 12 and 24 months post procedure)
  • TLF(30 days post procedure)
  • Cardiac Death Rate(30 days, 12 months and 24 months post procedure)
  • Fluoroscopy Time, during Index Procedure(End of the index procedure)
  • Minimal Lumen Area by IVUS (IVUS substudy)(End of the index procedure)
  • Stent Thrombosis Events Rate(30-day, 12-month and 2 year post-procedure)
  • Index Procedure Duration(End of the index procedure)
  • Acute Stent Malappositon by IVUS (IVUS Substudy)(End of the index procedure)

Study Sites (4)

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