Post-Approval Study Protocol of the St. Jude Medical Trifecta Valve

NCT01514162 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 245

Last updated 2019-02-15

Study results available
· View outcomes & findings →

Summary

To further evaluate the long term clinical safety and effectiveness of the Trifecta valve

Conditions

  • Heart Valve Diseases

Interventions

DEVICE

Trifecta valve

surgical replacement of aortic valve

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
2012-02-29
Primary Completion
2014-10-31
Completion
2014-10-31

Countries

  • United States

Study Locations

More Related Trials

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 NCT01514162 on ClinicalTrials.gov