The Effect of Centralization on Medial Meniscal Extrusion for Medial Meniscus Posterior Root Tear Repair

NCT07388290 — Not applicable, Enrolling by invitation, 54 participants, Mayo Clinic

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RegistryNCT07388290
StatusEnrolling by invitation
PhaseNot applicable
Study typeInterventional; randomized, parallel, masking: none, treatment
Enrollment54 (Estimated)
SponsorMayo Clinic (Other)
ConditionsMeniscus Tear
InterventionsMedial meniscus posterior root tear (MMPRT) repair with meniscus centralization, Medial meniscus posterior root tear (MMPRT) repair without meniscus centralization (Procedure)
Datesstart 2026-02-17, primary completion 2028-09-01 (estimated), completion 2030-03-01 (estimated), first posted 2026-02-05, last updated 2026-04-13
Locations3 sites in United States

Related Papers Related Patents Related Grants Related Experts
All trials for Meniscus Tear All trials of Medial meniscus posterior root tear (MMPRT) repair with meniscus centralization All trials of Medial meniscus posterior root tear (MMPRT) repair without meniscus centralization

-Summary

The purpose of this research is to determine if meniscus root repair with or without centralization will have an impact on postoperative pain, function, activity levels, patient satisfaction, and incidence of revision meniscus surgery.

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+Arms and interventions

ArmTypeInterventionsDescription
Repair with meniscus centralizationExperimentalProcedure: Medial meniscus posterior root tear (MMPRT) repair with meniscus centralizationMedial meniscus posterior root tear (MMPRT) surgical repair with meniscus centralization
Repair without centralizationActive comparatorProcedure: Medial meniscus posterior root tear (MMPRT) repair without meniscus centralizationMedial meniscus posterior root tear (MMPRT) surgical repair without centralization
  • Medial meniscus posterior root tear (MMPRT) repair with meniscus centralization (Procedure): The centralization technique involves placement of 1.8-mm Knotless FiberTak suture anchors along the periphery of the tibial plateau, starting from the posteromedial corner and progressing anteriorly. The anchors are deployed using a curved drill guide, and sutures are passed in a mattress configuration to re-tension the meniscotibial ligament to centralize the meniscus. Once centralization is complete, the posterior root tear is repaired using an anatomic suture anchor for aperture medial meniscus root fixation.
  • Medial meniscus posterior root tear (MMPRT) repair without meniscus centralization (Procedure): The posterior root tear is repaired using an anatomic suture anchor for aperture medial meniscus root fixation.

+Outcome measures

Primary outcomes

  • Meniscus extrusion measurement [Baseline (Preoperatively), 6 months]: Meniscus extrusion is measured in millimeters (mm) on coronal MRI at the level of the tibial spine

Secondary outcomes

  • Change in Kellgren-Lawrence grade on X-ray [Baseline (Screening), 12 months, 24 months]: The Kellgren-Lawrence (KL) system is a 0-4 scale used to grade the severity of knee osteoarthritis (OA) based on X-ray. It ranges from Grade 0 (no changes) to Grade 4 (severe).
  • Change in Tegner Activity Score [Baseline, 2 weeks, 6 weeks, 3 months, 6 months, 12 months, 24 months]: The Tegner Activity Questionnaire is a 1-item questionnaire rating physical activity from 0 (Disabled) to 10 (Elite competitive athlete). Total scores range from 0 - 10, with higher scores indicating a higher level of activity.
  • Change in Visual Analog Scale (VAS) Questionnaire score [Baseline, 2 weeks, 6 weeks, 3 months, 6 months, 12 months, 24 months]: The VAS is a 2-item questionnaire assessing pain using a scale of 0 (No pain) to 10 (Worst pain). Total scores range from 0 - 10, lower scores indicating lower pain and higher scores indicating greater pain.
  • Change in Knee Injury and Osteoarthritis Outcome Score Jr. (KOOS, JR) Questionnaire score [Baseline, 2 weeks, 6 weeks, 3 months, 6 months, 12 months, 24 months]: The KOOS JR is a questionnaire designed to measure outcomes for patients with knee replacements. Questions focus on knee stiffness, pain, and function for daily activities and are assessed on a 5 point Likert-scale between 0 (None) and 4 (Extreme). Total scores range from 0 - 28, with higher scores indicating a greater impact of pain on daily functioning.
  • Change in International Knee Documentation Committee (IKDC) Questionnaire score [Baseline, 2 weeks, 6 weeks, 3 months, 6 months, 12 months, 24 months]: The International Knee Documentation Committee (IKDC) Subjective Knee Evaluation assesses overall function over 3 domains: symptoms, athletic activity, and knee function. Higher scores indicate higher levels of function and lower levels of symptoms.
  • Change in Likert Knee Questionnaire score [Baseline, 2 weeks, 6 weeks, 3 months, 6 months, 12 months, 24 months]: The Likert Knee Questionnaire is a 1-item survey asking the patient to rate knee pain post-surgery on a Likert scale where 0 (Much better than before surgery) and 5 (Much worse than before surgery).
  • Surgery Satisfaction Questionnaire [2 weeks, 6 weeks, 3 months, 6 months, 12 months, 24 months]: The Surgery Satisfaction Questionnaire is a 1-item survey asking the patient to rate satisfaction with knee surgery on a Likert scale where 0 (Not at all) and 10 (Most Satisfied).

+Eligibility

Sex: All, ages: 18 Years to 65 Years

Inclusion Criteria:

* Type 2 Medial Meniscus Posterior Root Tear demonstrated on MRI
* Notable extrusion (>3 mm) on preoperative MRI
* Patient able to consent for themselves
* Patient agrees to comply with trial schedules and plan

Pre-operative Exclusion:

* Concomitant ligamentous or meniscal procedures
* Meniscal extrusion > 6 mm on pre-operative MRI
* Kellgren-Lawrence grade > 2
* Varus malalignment > 10 degrees
* Asymmetric varus alignment > 5 degrees
* Varus thrust while weightbearing
* Grade 3 bipolar medial compartment changes (isolated grade 3 changes on single articular surface with ≤ grade 2 changes on the opposing surface remains eligible)
* Previous surgery of the affected knee
* Associated fractures requiring surgery
* Concurrent Vascular injuries
* Hypermobility/Ehlers-Danlos Syndrome
* Inflammatory or autoimmune disease
* Severe mental/physical disability precluding post operative rehabilitation demands
* Contraindications to MRI
* Pregnant women

Arthroscopy Inclusion Criteria:

* Complete radial tears within 9 mm of medial meniscus posterior root
* ICRS Grade 3 or better

Arthroscopy Exclusion Criteria:

* Requiring concomitant procedures other than MMPRT
* ICRS Grade 4 changes

+Locations (3)

FacilityCityCountryStatus
The Steadman ClinicWest Vail, ColoradoUnited States
Hospital for Special Surgery at Naples Comprehensive Health (HSS at NCH),Naples, FloridaUnited States
Mayo ClinicRochester, MinnesotaUnited States

+Investigators