MedTrace Logo

Zimmer® MotionLoc® in Distal Tibia Fractures

NCT02717546 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 32

Last updated 2021-08-04

Study results available
· View outcomes & findings →

Summary

The objective of this observational prospective study is to systematically document the clinical outcomes of Zimmer MotionLoc Screws for Periarticular Locking Plate System applied to distal tibia fracture treatment and confirm safety and performance of the screws.

Conditions

  • Distal Tibia Fractures

Interventions

DEVICE

Zimmer MotionLoc Screw

Patients with distal tibia fractures (AO 43-A and C) requiring surgical intervention eligible for locked plating.

Sponsors & Collaborators

  • Zimmer Biomet

    lead INDUSTRY

Principal Investigators

  • Kacy Arnold, RN MBA · Zimmer Biomet

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2016-02-29
Primary Completion
2019-12-05
Completion
2020-01-15

Countries

  • United States
  • Australia
  • Italy
  • South Korea
  • United Kingdom

Study Locations

More Related Trials

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 NCT02717546 on ClinicalTrials.gov