MedTrace Logo

Scorpio Non Restricted Geometry (NRG) Study in Japan

NCT02552082 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 150

Last updated 2018-09-17

No results posted yet for this study

Summary

The purpose of this study is to evaluate the range of motion (ROM), mid-flexion stability (gap balance), and implant position (size and angle) for the Scorpio NRG device. Relationship between these parameters and clinical outcomes will be evaluated as well as the importance of rotational tolerance. It is expected that the Scorpio NRG will have good clinical outcomes and perform the same or better than other total knee implants.

Conditions

Interventions

DEVICE

Scorpio NRG posterior stabilized (PS)

Sponsors & Collaborators

  • Stryker Japan K.K.

    lead INDUSTRY

Eligibility

Min Age
20 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2015-06-30
Primary Completion
2018-03-31
Completion
2018-03-31

Countries

  • Japan

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 NCT02552082 on ClinicalTrials.gov