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Clinical Trials/NCT01405729
NCT01405729
Completed
N/A

Medial Patellofemoral Ligament Reconstruction: A Review of Technique, Accuracy, and Outcome

University of Utah1 site in 1 country13 target enrollmentMay 2010

Overview

Phase
N/A
Intervention
Not specified
Conditions
Healthy
Sponsor
University of Utah
Enrollment
13
Locations
1
Primary Endpoint
Radiograph measurements
Status
Completed
Last Updated
12 years ago

Overview

Brief Summary

The purpose of this retrospective study was to determine the accuracy of femoral tunnel placement utilizing Redfern et al's radiographic method for anatomic femoral attachment during MPFL reconstruction in addition to the resultant outcome.

Detailed Description

Reconstruction of the medial patellofemoral ligament (MPFL) has been shown to be an effective treatment for recurrent patellar instability, There has been some concern in the literature about the accuracy of femoral tunnel placement and the effect that it might have on patient outcomes. The investigators evaluated the accuracy of MPFL placement using an intraopetative fluoroscopy technique and to assess subsequent patient outcomes. All patients undergoing MPFL reconstruction using an intraoperative fluoroscopically guided technique between 2005 and 2010 were identified. A retrospective review of their charts and radiographs were performed and the subjects were brought back for a follow up exam, radiographic series, and Kujala questionaire.

Registry
clinicaltrials.gov
Start Date
May 2010
End Date
December 2013
Last Updated
12 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Robert Burks

M.D.

University of Utah

Eligibility Criteria

Inclusion Criteria

  • Patients having undergone the MPFL procedure, starting January 1, 2005 through February 3, 2010
  • Minimum follow up of 24 months

Exclusion Criteria

  • Pregnant women
  • Under 18 years of age
  • Previously undergone prior MPFL surgery
  • Participated in any previous research studies involving the use of ionizing radiation (either radioisotopes or diagnostic x-rays during the past 12 months.
  • The participant should not volunteer for other research studies involving the use of ionizing radiation within 12 months of completing the current study.

Outcomes

Primary Outcomes

Radiograph measurements

Time Frame: 5 years

Study Sites (1)

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