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Comparison of Function and Fit of Standard and Gender-Specific CR High-Flex Total Knee Prostheses

NCT00916968 · Status: COMPLETED · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 146

Last updated 2009-07-02

No results posted yet for this study

Summary

The purpose of this prospective, randomized study was to compare functional outcome, radiographic results, range of motion, patients satisfaction, and fit of the femoral component in patients receiving either a standard posterior cruciate-retaining high-flexion (CR-flex) and gender-specific CR-flex total knee prostheses.

Conditions

Interventions

DEVICE

Standard CR-Flex total knee

total knee implant used for joint replacement surgery of the knee

DEVICE

Gender specific CR-Flex

TKA by Gender specific Nexgen CR-Flex

Sponsors & Collaborators

  • Ewha Womans University

    lead OTHER

Principal Investigators

  • Yoowang Choi, MD · Ewha Womans University Mokdong Hospital

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
TRIPLE
Model
PARALLEL

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2007-02-28
Primary Completion
2007-05-31
Completion
2009-05-31

Countries

  • South Korea

Study Locations

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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 NCT00916968 on ClinicalTrials.gov