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Medial Patellofemoral Ligament Reconstruction With or Without Lateral Retinaculum Release

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ClinicalTrials.gov Identifier: NCT01719666
Recruitment Status : Recruiting
First Posted : November 1, 2012
Last Update Posted : May 23, 2017
Sponsor:
Information provided by (Responsible Party):
Hospices Civils de Lyon

December 22, 2011
November 1, 2012
May 23, 2017
November 2011
November 2020   (Final data collection date for primary outcome measure)
Patellar tilt measurement [ Time Frame: 2 years of follow up ]
IKDC score, patellar tilt measurement on x-rays and CT-scan
Same as current
Complete list of historical versions of study NCT01719666 on ClinicalTrials.gov Archive Site
rate of complications [ Time Frame: 2 years of follow up ]
Same as current
Not Provided
Not Provided
 
Medial Patellofemoral Ligament Reconstruction With or Without Lateral Retinaculum Release
Randomized Control Trial on Lateral Retinaculum Release in MPFL Reconstruction
The investigators hypothesis is lateral retinaculum release has no effect on treatment of Patellar Recurrent Dislocation with Medial Patellofemoral Ligament (MPFL) reconstruction.
Not Provided
Interventional
Not Applicable
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: None (Open Label)
Primary Purpose: Treatment
Episodic Patellar Dislocation
  • Procedure: MPFL reconstruction and lateral retinaculum release
    MPFL is performed with a standard technique using gracilis tendon. A tunnel is performed at the femoral part with a bioabsorbable screw fixation and 2 bundles with suture fixation at the patellar side
  • Procedure: conventional surgery
    conventional surgery: MPFL reconstruction
  • isolated MPFL reconstruction
    Intervention: Procedure: conventional surgery
  • Experimental: MPFL reconstruction and Lateral retinaculum release
    Intervention: Procedure: MPFL reconstruction and lateral retinaculum release
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Recruiting
140
Same as current
November 2020
November 2020   (Final data collection date for primary outcome measure)

Inclusion Criteria:

  • age between 18yo and 45yo
  • indication for MPFL reconstruction
  • unilateral or bilateral indication

Exclusion Criteria:

  • indication for bony procedures
  • previous surgery for PF disorders
  • patient refusal
Sexes Eligible for Study: All
18 Years to 45 Years   (Adult)
No
Contact: Elvire SERVIEN, MD,PhD +33 4 72 26 92 51 elvire.servien@chu-lyon.fr
France
 
 
NCT01719666
2010.651
No
Not Provided
Not Provided
Hospices Civils de Lyon
Hospices Civils de Lyon
Not Provided
Not Provided
Hospices Civils de Lyon
May 2017

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP