St. Jude Medical Percutaneous Mitral Valve Repair Study

NCT01500148 · Status: COMPLETED · Phase: PHASE1 · Type: INTERVENTIONAL · Enrollment: 2

Last updated 2019-02-04

No results posted yet for this study

Summary

The purpose of this proof-of-concept study is to assess the relative safety and feasibility of the SJM Percutaneous Mitral Valve Repair (PMVr) Device.

Conditions

  • Mitral Valve Prolapse

Interventions

DEVICE

PMVr procedure (SJM Percutaneous Mitral Valve Repair (PMVr)

A maximum of ten (10) subjects will receive a percutaneous mitral valve clip procedure.

Sponsors & Collaborators

  • Abbott Medical Devices

    lead INDUSTRY

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2011-12-31
Primary Completion
2012-06-30
Completion
2012-08-31

Countries

  • United Kingdom

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 NCT01500148 on ClinicalTrials.gov