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Comparative Study of Osteosynthesis for Chevron Osteotomy of Hallux Valgus Using Degradable Versus Non-degradable Metallic Device

NCT01535144 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 26

Last updated 2012-03-01

No results posted yet for this study

Summary

The purpose of the study is to show the equivalence of a new degradable metallic device to a non-degradable metallic device in patients with Hallux Valgus.

Conditions

  • Hallux Valgus

Interventions

DEVICE

Fracture compressing screw ZfW 102 Königsee Implantate GmbH

Comparison of two metallic implantable fracture compressing screws

DEVICE

Fracture compressing screw titanium Königsee Implantate GmbH

Comparison of two metallic implantable fracture compressing screws

Sponsors & Collaborators

  • Syntellix AG

    lead INDUSTRY

Principal Investigators

  • Henning Windhagen, Prof., MD · Clinic for Orthopaedic Surgery (in the Annastift Hospital)

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
40 Years
Max Age
79 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2010-02-28
Primary Completion
2012-02-29
Completion
2012-02-29

Countries

  • Germany

Study Locations

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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 NCT01535144 on ClinicalTrials.gov