Comparison of Tibial Plateau Fractures Outcomes Treated With Non-locking and Locking Plate

January 11, 2014 updated by: Amin Nemati, Isfahan University of Medical Sciences
this study will perform to compare the results and functional outcomes of tibial plateau fractures treated with non-locking and locking plate fixation.

Study Overview

Status

Unknown

Conditions

Intervention / Treatment

Study Type

Interventional

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

  • Iran, Islamic Republic of
      • Isfahan, Iran, Islamic Republic of, 8174673461
        • Recruiting
        • Vice Chancellery for Research of Isfahan University of Medical Sciences, Isfahan, Iran
        • Contact:
          • Amin Nemati, Orthopedic surgery resident

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

19 years to 60 years (Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • unilateral closed tibia plateau fracture

Exclusion Criteria:

  • patients who have been treated with casting or screw
  • history of diabetes mellitus
  • evidences of pathological fractures

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Treatment

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Locking plate
Device: Locking plate
Active Comparator: Non-Locking plate
Device: Non-Locking plate

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Time Frame
knee society knee score
Time Frame: ten months after surgery
ten months after surgery

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Isfahan University of Medical Sciences

Investigators

  • Study Director: Mohammad Ali Tahririan, Orthopedic surgeon, Department of Orthopedics, Kashani hospital, Isfahan University of Medical sciences, Isfahan, Iran
  • Principal Investigator: Mohsen Derakhshan, Orthopedic surgery resident, Department of Orthopedics, Kashani hospital, Isfahan University of Medical sciences, Isfahan, Iran

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Primary Completion (Anticipated)

April 1, 2014

Study Registration Dates

First Submitted

January 11, 2014

First Submitted That Met QC Criteria

January 11, 2014

First Posted (Estimate)

January 14, 2014

Study Record Updates

Last Update Posted (Estimate)

January 14, 2014

Last Update Submitted That Met QC Criteria

January 11, 2014

Last Verified

January 1, 2014

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • 392120

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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