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

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
 
ClinicalTrials.gov Identifier: NCT02035917
Recruitment Status : Unknown
Verified January 2014 by Amin Nemati, Isfahan University of Medical Sciences.
Recruitment status was:  Recruiting
First Posted : January 14, 2014
Last Update Posted : January 14, 2014
Sponsor:
Information provided by (Responsible Party):
Amin Nemati, Isfahan University of Medical Sciences

Study Description
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Brief Summary:
this study will perform to compare the results and functional outcomes of tibial plateau fractures treated with non-locking and locking plate fixation.

Condition or disease Intervention/treatment Phase
Tibial Fracture Device: Locking plate Device: Non-Locking plate Not Applicable

Study Design
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Study Type : Interventional  (Clinical Trial)
Primary Purpose: Treatment
Estimated Primary Completion Date : April 2014

Resource links provided by the National Library of Medicine


Arms and Interventions
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Arm Intervention/treatment
Experimental: Locking plate Device: Locking plate
Active Comparator: Non-Locking plate Device: Non-Locking plate


Outcome Measures
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Primary Outcome Measures :
  1. knee society knee score [ Time Frame: ten months after surgery ]

Eligibility Criteria
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Information from the National Library of Medicine

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Ages Eligible for Study:   19 Years to 60 Years   (Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Criteria

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
Contacts and Locations
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Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT02035917


Contacts
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Contact: Amin Nemati, Orthopedic surgery resident 00989131009918 nemati@med.mui.ac.ir

Locations
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Iran, Islamic Republic of
Vice Chancellery for Research of Isfahan University of Medical Sciences, Isfahan, Iran Recruiting
Isfahan, Iran, Islamic Republic of, 8174673461
Contact: Amin Nemati, Orthopedic surgery resident         
Sponsors and Collaborators
Isfahan University of Medical Sciences
Investigators
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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
More Information
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Responsible Party: Amin Nemati, Orthopedic surgery resident,Orthopedic department,Alzahra hospital,Isfahan University of Medical Sciences,Isfahan,Iran, Isfahan University of Medical Sciences
ClinicalTrials.gov Identifier: NCT02035917    
Other Study ID Numbers: 392120
First Posted: January 14, 2014    Key Record Dates
Last Update Posted: January 14, 2014
Last Verified: January 2014
Additional relevant MeSH terms:
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Fractures, Bone
Tibial Fractures
Wounds and Injuries
Leg Injuries