MedTrace Logo

Observational Patient Registry of the Dynamic Locking Screws

NCT02656628 · Status: WITHDRAWN · Type: OBSERVATIONAL

Last updated 2016-01-21

No results posted yet for this study

Summary

The purpose of this multi-center patient registry is to obtain first clinical results and to assess short and mid-term clinical outcome data of patients treated with DLS.

Conditions

  • Proximal or Diaphyseal Humerus Fracture
  • Diaphyseal or Distal Femur Fracture
  • Diaphyseal, Distal or Proximal Tibia Fracture

Interventions

DEVICE

Dynamic Locking Screw 3.7mm and 5.0mm

Treatment with DLS and locked plate constructs (small or large fragments)

Sponsors & Collaborators

  • Synthes Australia Pty Ltd

    collaborator INDUSTRY

  • Synthes GmbH

    lead INDUSTRY

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2015-05-31
Primary Completion
2016-11-30
Completion
2016-11-30

Countries

  • Australia

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 NCT02656628 on ClinicalTrials.gov