Overview

This trial is active, not recruiting.

Conditions knee stability, patella luxation
Treatment anchor fixation
Sponsor Aarhus University Hospital
Start date January 2009
End date December 2019
Trial size 60 participants
Trial identifier NCT02180685, Danish EC 1-10-72-194-14

Summary

The purpose of this present study is to determine which surgery technic provides the best clinical outcome after medial patellofemoral ligament reconstruction comparing suture anchors and screw fixation in medial femoral condyle.

United States No locations recruiting
Other Countries No locations recruiting

Study Design

Allocation randomized
Intervention model parallel assignment
Masking single blind (subject)
Primary purpose health services research
Arm
(Other)
Medial fixation of the reconstruction at the medial femural condyle with suture anchors.
anchor fixation
(Other)
Medial fixation of the reconstruction at the medial femural condyle with a screw.
anchor fixation

Primary Outcomes

Measure
Evaluation of subjective symptoms with a patient reported outcome score
time frame: Baseline, 6 months 12 Months, 24 months

Secondary Outcomes

Measure
Patient reported outcome scores
time frame: Baseline, 6 months 12 Months, 24 months
Patient reported outcome scores
time frame: Baseline, 6 months 12 Months, 24 months
Re-operation rate
time frame: Baseline, 6 months 12 Months, 24 months

Eligibility Criteria

Male or female participants from 18 years up to 40 years old.

Inclusion Criteria: - patella luxation, more than 2 times Exclusion Criteria: - cartilage damage (grad 3)

Additional Information

Official title Reconstruction of the Medial Patellofemoral Ligament - A Randomised Controlled Trial Comparing Two Surgery Technics
Trial information was received from ClinicalTrials.gov and was last updated in July 2016.
Information provided to ClinicalTrials.gov by Aarhus University Hospital.