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Surgical Plate Osteosynthesis of Distal Radius Fractures

NCT00205998 · Status: TERMINATED · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 450

Last updated 2007-04-27

No results posted yet for this study

Summary

Primary objective of the study is to demonstrate specific indications for the

surgical treatment of distal radius fractures using the locking compression

plate.

Conditions

  • Distal Radius Fractures

Interventions

DEVICE

Locking Compression Plate 2,4mm

DEVICE

Locking Compression Plate 3,5mm

Sponsors & Collaborators

  • Synthes Inc.

    collaborator INDUSTRY

  • AO Hand Expert Group

    collaborator OTHER

  • AO Clinical Investigation and Publishing Documentation

    lead OTHER

Principal Investigators

  • Andreas W Wentzensen, Prof. MD · BG-Unfallklinik Ludwigshafen

  • Jesse B Jupiter, Prof. MD · Harvard Medical School (HMS and HSDM)

  • Peter G De Boer, F.R.C.S. · York District Hospital

Study Design

Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
80 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2001-12-31
Completion
2005-12-31

Countries

  • United States
  • Germany
  • United Kingdom

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 NCT00205998 on ClinicalTrials.gov