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Clinical Trials/NCT00816647
NCT00816647
Terminated
N/A

A Prospective Randomized Study of Medial Patellofemoral Ligament Reconstruction Compared With Medial Reefing

Finnish Defense Forces1 site in 1 country50 target enrollmentDecember 2008

Overview

Phase
N/A
Intervention
Not specified
Conditions
Patella-Dislocation
Sponsor
Finnish Defense Forces
Enrollment
50
Locations
1
Primary Endpoint
Recurrent patellar instability
Status
Terminated
Last Updated
14 years ago

Overview

Brief Summary

The operative management of chronic patellar instability has been controversial. Medial patellofemoral ligament reconstruction has gained success recently and might be superior to other soft-tissue procedures. The objective of this prospective study was to compare the clinical outcome after medial patellofemoral ligament reconstruction compared with medial reefing for chronic patellar instability.

Detailed Description

Many of the previous studies on medial patellofemoral ligament (MPFL) reconstruction for patellar instability have been difficult to interpret, either because the study setting has included both first-time and recurrent dislocations, or because a lack of control group. Moreover, several studies have enrolled patients with a wide age range, and the majority of the studies have employed retrospective and nonrandomized study designs. Therefore the investigators designed a prospective, randomized study with the primary goal to compare the outcome after MPFL reconstruction with medial reefing for chronic patellar instability. The distance between tibial tubercle and trochlear groove is measured on MRI and corrected if it exceeds 17mm. Primary outcome measure is the occurrence of recurrent objective and subjective patellar instability. The second goal is to evaluate the development of articular cartilage lesions within the patellofemoral joint, and assess clinical scores.

Registry
clinicaltrials.gov
Start Date
December 2008
End Date
June 2011
Last Updated
14 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Finnish Defense Forces

Eligibility Criteria

Inclusion Criteria

  • Chronic patellar instability (more than 2 dislocations)
  • Minimum 6 months nonoperative treatment

Exclusion Criteria

  • Severe PF OA
  • Acute patellar dislocation

Outcomes

Primary Outcomes

Recurrent patellar instability

Time Frame: 2 years

Secondary Outcomes

  • Patellofemoral osteoarthrosis progression.(2 years)

Study Sites (1)

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