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Safety and Efficacy Study of the Sorin 3D Annuloplasty Ring For Mitral Repair

NCT00567853 · Status: COMPLETED · Phase: PHASE3 · Type: INTERVENTIONAL · Enrollment: 278

Last updated 2015-01-26

No results posted yet for this study

Summary

The purpose of this study is to collect data on the effectiveness and clinical outcomes of the MEMO 3D Annuloplasty ring as used for mitral valve repair.

Conditions

  • Mitral Valve Regurgitation

Interventions

DEVICE

Implantation of the MEMO 3D Annuloplasty Ring

Implantation of the MEMO 3D Annulopalsty Ring for mitral valve repair.

Sponsors & Collaborators

  • Sorin Group USA, Inc.

    lead INDUSTRY

Principal Investigators

  • Clark Hargrove, M.D. · University of Pennsylvania Presbyterian Medical Center

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2007-08-31
Primary Completion
2013-06-30
Completion
2013-06-30

Countries

  • United States
  • Canada

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00567853 on ClinicalTrials.gov