Medial Retinacular Plication Versus Medial Patellofemoral Ligament Reconstruction for Recurrent Patellar Instability

Sponsor
Meir Medical Center (Other)
Overall Status
Recruiting
CT.gov ID
NCT02480959
Collaborator
Rambam Health Care Campus (Other), Hadassah Medical Organization (Other), Assaf-Harofeh Medical Center (Other), Soroka University Medical Center (Other)
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Study Details

Study Description

Brief Summary

The purpose of this study is to determine whether medial patellofemoral ligament reconstruction results in superior functional outcomes compared to medial retinacular plication surgery in cases of recurrent patellar instability.

Condition or Disease Intervention/Treatment Phase
  • Procedure: Surgical treatment for recurrent patellar instability
N/A

Detailed Description

Patients with recurrent lateral patellar instability will be assigned to undergo one of two surgical approaches aimed to prevent recurrent patellar instability and result in improvement in function. One surgical approach will be medial retinacular plication with multiple stitches while the other surgical approach will include medial patellofemoral ligament reconstruction using a hamstring tendon graft. Prior to surgery, and then during follow-up after surgery as well as at the completion of minimum two years follow-up after surgery, patients will be asked to complete subjective functional questionaires that will rate their knee function, and to undergo detailed physical examination and objective functional tests that will quantify the success of surgery. The outcomes of the surgical treatment options will be compared to determine whether medial patellofemoral ligament reconstruction results in superior function and patient subjective satisfaction compared to medial retinacular plication only.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
30 participants
Allocation:
Non-Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Functional Outcome of Surgical Treatment for Recurrent Patellar Instability: A Prospective Comparative Study Between Medial Retinacular Plication Versus Medial Patellofemoral Ligament Reconstruction
Actual Study Start Date :
Aug 1, 2015
Anticipated Primary Completion Date :
Dec 1, 2022
Anticipated Study Completion Date :
Dec 1, 2022

Arms and Interventions

Arm Intervention/Treatment
Other: Medial plication

Patient undergoing surgical treatment for recurrent patellar instability that includes medial retinacular plication

Procedure: Surgical treatment for recurrent patellar instability
Either medial plication or MPFL reconstructuion surgery

Other: MPFL reconstruction

Patient undergoing surgical treatment for recurrent patellar instability that includes medial patellofemoral ligament reconstruction using a tendon graft

Procedure: Surgical treatment for recurrent patellar instability
Either medial plication or MPFL reconstructuion surgery

Outcome Measures

Primary Outcome Measures

  1. Kujala knee outcome score [Between two and five years after surgery]

    A validated international outcome score that evaluates knee functional outcome in relation to patellofemoral symptoms

Secondary Outcome Measures

  1. International Knee Documentation Committee subjective outcome score [Between two and five years after surgery]

    A validated international outcome score that evaluates general knee functional outcome

  2. Tenger activity level score [Between two and five years after surgery]

    A validated international outcome score that evaluates highest level of sports activity

  3. Marx activity level score [Between two and five years after surgery]

    A validated international outcome score that evaluates highest level of sports activity

  4. Visual Analogue Scale [Between two and five years after surgery]

    A validated international scale that evaluates level of pain

  5. Single hop test [Between two and five years after surgery]

    Evaluates limb asymmetry index between operated and nonoperated limbs during a single legged hop for distance

  6. Side-to-side hop test [Between two and five years after surgery]

    Evaluates limb asymmetry index between operated and nonoperated limbs performing side to side repetaed hops during 30 seconds

  7. Patellar apprehension test [Between two and five years after surgery]

    Evaluates normal patellar tracking and patient's feeling of subjective comfort while the examiner apply a provocative force that translates the patella lateraly

  8. Infectious event of the operated knee documented by number of events that required antibiotics treatment with or without joint lavage [Immediately after surgery, for the duration of hospital stay, and until expected time of 1 month]

    Infection of the surgical site as a severe complication of surgery, requirng antibiotics with or without joint lavage

Eligibility Criteria

Criteria

Ages Eligible for Study:
15 Years to 35 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Recurrent lateral patellar instability has been described by the patient
Imaging criteria include:
  • TT-TG distance (on CT or MRI) is between 10-20 mm

  • Insall-Salvati Index is between 0.9 - 1.2

  • Trochlea angle is lower than 145 degrees

Exclusion Criteria:
  • Only a single event of lateral patellar instability occured
Imaging criteria include:
  • TT-TG distance (on CT or MRI) is below 10 mm or above 20 mm

  • Insall-Salvati Index is below 0.9 or above 1.2

  • Trochlea angle is above 145 degrees

  • Other concomitant intra-articular patholgies, injuries, and surgeries, besides the patella instability, with were recorded at the lower limbs and did not uneventfuly healed, and as a result cause dysfunction of the lower limbs

  • Significant ligamentous injuries of the knees, including cruciate and collateral injuries, as well as meniscal injuries that interfere with function

Contacts and Locations

Locations

Site City State Country Postal Code
1 Meir Medical Center Kfar Saba Israel 44281

Sponsors and Collaborators

  • Meir Medical Center
  • Rambam Health Care Campus
  • Hadassah Medical Organization
  • Assaf-Harofeh Medical Center
  • Soroka University Medical Center

Investigators

  • Principal Investigator: IFTACH HETSRONI, M.D., Meir Medical Center
  • Principal Investigator: DROR LINDNER, M.D., Assaf-Harofeh Medical Center
  • Principal Investigator: IDAN ILSAR, M.D., Hadassah Medical Organization
  • Principal Investigator: MAZEN FALAH, M.D., Rambam Health Care Campus
  • Principal Investigator: NASSIM ALKRINAWI, M.D., Soroka University Medical Center

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Meir Medical Center
ClinicalTrials.gov Identifier:
NCT02480959
Other Study ID Numbers:
  • 0041-15-MMC
First Posted:
Jun 25, 2015
Last Update Posted:
Mar 4, 2020
Last Verified:
Mar 1, 2020
Additional relevant MeSH terms:

Study Results

No Results Posted as of Mar 4, 2020