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A Single-Center, Epidemiological Study of the Survivorship of the DePuy Sigma HP Unicompartmental Knee Prosthesis

NCT01656694 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 300

Last updated 2018-03-22

No results posted yet for this study

Summary

This study will be conducted to assess the survivorship of a particular prosthesis used in unicompartmental knee arthroplasties. Patients undergoing this procedure have been diagnosed with isolated medial or lateral compartmental arthritis and have failed conservative treatment. The patients received a unicompartmental knee replacement using the Sigma® HP Partial Knee System.

Conditions

Interventions

DEVICE

DePuy Sigma HP Partial Knee

Sponsors & Collaborators

  • DePuy Orthopaedics

    collaborator INDUSTRY

  • Mississippi Sports Medicine and Orthopaedic Center

    lead OTHER

Principal Investigators

  • Jeff D Almand, MD · Mississippi Sports Medicine and Orthopaedic Center

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2012-08-31
Primary Completion
2015-12-31
Completion
2016-12-31

Countries

  • United States

Study Locations

More Related Trials

Entities

Diseases

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 NCT01656694 on ClinicalTrials.gov