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Functional and Quality of Life Outcomes Following Viscosupplementation for Knee Osteoarthritis

NCT01447303 · Status: TERMINATED · Type: OBSERVATIONAL · Enrollment: 43

Last updated 2014-01-27

No results posted yet for this study

Summary

This study will compare changes in outcomes following viscosupplementation for knee osteoarthritis.

Conditions

Interventions

OTHER

Subject outcomes following viscosupplementation of the knee

The study subject outcomes (WOMAC, VAS, SF-36, Chair rise, Stair climb, Six minute walk and Gait analysis) measured at 1, 3, 6 and 12 months following viscosupplementation of the knee

Sponsors & Collaborators

  • University of Florida

    lead OTHER

Principal Investigators

  • Heather K Vincent, Ph.D. · University of Florida Department of Orthopaedics and Rehabilitation

Eligibility

Min Age
21 Years
Max Age
85 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2009-08-31
Primary Completion
2013-11-30
Completion
2013-11-30

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 NCT01447303 on ClinicalTrials.gov