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UnknownNCT02543489

Flex Intramedullary Rod Study

A Prospective, Post-market, Multi-center Comparative Study of the Efficacy of Flex Intramedullary(IM) Rod in Terms of Range of Motion (ROM) Improvement.

Status
Unknown
Phase
N/A
Study type
Interventional
Enrollment
100 (actual)
Sponsor
Stryker Japan K.K. · Industry
Sex
All
Age
20 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to compare the effect of post-operative ROM between Flex IM rod and Rigid IM rod, to collect bone morphology of Japanese lower extremity and to research the incidence of overhung with Flex IM rod.

Conditions

Interventions

TypeNameDescription
DEVICEFlex IM rod

Timeline

Start date
2012-12-01
Primary completion
2019-09-01
Completion
2019-09-01
First posted
2015-09-07
Last updated
2018-09-14

Locations

3 sites across 1 country: Japan

Source: ClinicalTrials.gov record NCT02543489. Inclusion in this directory is not an endorsement.

Flex Intramedullary Rod Study (NCT02543489) · Clinical Trials Directory