Meniscal Root Tears: Evaluation Using an Ultrahigh MRI

Sponsor
Twin Cities Orthopedics (Other)
Overall Status
Recruiting
CT.gov ID
NCT05088525
Collaborator
(none)
30
1
2
24.3
1.2

Study Details

Study Description

Brief Summary

Meniscal root tears have been recently recognized to be one of the most common causes for the progression of arthritis in relatively young patients. The purpose of the study will be to assess if the addition of a transtibial peripheral stabilization suture helps to decrease both meniscal extrusion and if it helps to decrease the progression of osteoarthritis of the medial compartment of the knee in the early timeframe postoperatively.

Condition or Disease Intervention/Treatment Phase
  • Procedure: MRI
N/A

Detailed Description

Studies have reported that the most common reason why patients require total knee arthroplasty before the age of 60 is a neglected or meniscectomized medial meniscus root tear. Overall, it has been noted that meniscal root repairs are cost effective and that the outcomes of meniscus root repairs are demonstrating patients have a significant improvement of their preoperative symptoms up to several years after surgery. Because most centers have only been preforming meniscus root repairs over the last five to ten years, we are now starting to recognize why some of the repairs do not function as well as others. The number one reason appears to be due to a postoperative meniscus extrusion. Meniscus extrusion has been seen in up to 50% of postoperative patients, and biomechanical studies have demonstrated that the cushioning effect of the medial meniscus does not function as well when there is a meniscus extrusion present. New biomechanical studies have demonstrated that the addition of a peripheral stabilization suture at the far posteromedial aspect of the medial tibial plateau helps to hold the meniscus better in the joint and that it also results in a significant decrease in load on the medial compartment. However, clinical studies are lacking to date as to whether a peripheral stabilization suture may or may not improve the protected function of the medial meniscus, decreased extrusion, and potentially lead to a less amount of progression of osteoarthritis in the medial compartment of the knee.

Therefore, this study strives to both assess the ability of a meniscus root repair to slow down the progression of arthritis of the medial compartment of patients with a 7-Tesla MRI scanner and also to concurrently assess the ability of the usage of a transtibial peripheral stabilization suture to decrease or eliminate meniscal extrusion. The importance of this study is that if the peripheral stabilization suture is noted to both decrease the progression of arthritis and also to decrease the meniscus extrusion, it will be a significant step forward in the treatment of these complex meniscal tears.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
30 participants
Allocation:
Randomized
Intervention Model:
Single Group Assignment
Masking:
Single (Outcomes Assessor)
Primary Purpose:
Treatment
Official Title:
Meniscal Root Tears: Evaluating Meniscal Extrusion After Root Repair With and Without Transtibial Peripheral Stabilization Sutures Using Ultrahigh Magnetic Fields: A Randomized Controlled Trial
Actual Study Start Date :
Nov 20, 2020
Anticipated Primary Completion Date :
Dec 1, 2022
Anticipated Study Completion Date :
Dec 1, 2022

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: Two-tunnel meniscal root repair without a peripheral stabilization suture

Standard root repair surgery.

Procedure: MRI
MRI for standard of care meniscus root repair surgery - noting with an added stabilization suture if it is able to successfully slow down the progression of osteoarthritis versus a standard root repair surgery.

Experimental: Meniscal root repair with an additional transtibial peripheral stabilization suture

Meniscus root repair with an added stabilization suture

Procedure: MRI
MRI for standard of care meniscus root repair surgery - noting with an added stabilization suture if it is able to successfully slow down the progression of osteoarthritis versus a standard root repair surgery.

Outcome Measures

Primary Outcome Measures

  1. MRI [Pre-operatively]

    Musculoskeletal radiologist assessment of medial meniscus extrusion and cartilage specific sequences gathered

  2. MRI [6 months post-operatively]

    Musculoskeletal radiologist assessment of medial meniscus extrusion and cartilage specific sequences gathered

Secondary Outcome Measures

  1. visual analog scale (VAS) scores [pre-operatively and post-operatively at 3 and 6 months]

    Pain scale 0-100

  2. International Knee Documentation Committee (IKDC) [pre-operatively and post-operatively at 3 and 6 months]

    The questionnaire looks at 3 categories: symptoms, sports activity, and knee function. Scores are obtained by summing the individual items, then transforming the crude total to a scaled number that ranges from 0 to 100. The higher the score, better outcomes 87/87 = 100%

  3. Cincinnati Knee Rating System [pre-operatively and post-operatively at 3 and 6 months]

    Functional assessment based on 6 abilities important for participation in sports. The higher the score, better outcomes 100/100 = 100%

  4. Knee injury and Osteoarthritis Outcome Score (KOOS) [pre-operatively and post-operatively at 3 and 6 months]

    Assesses five outcomes: pain, symptoms, activities of daily living, sport and recreation function, and knee-related quality of life. The maximum score a patient can achieve is 100, indicating no knee problems.

  5. Tegner [pre-operatively and post-operatively at 3 and 6 months]

    the higher the score, better outcomes 100/100 = 100% The scale is numbered on a "0-10" format, with 1 being professional and 1 being a person who is disabled from knee issues.

  6. Lysholm Knee Scoring Scale [pre-operatively and post-operatively at 3 and 6 months]

    Consists of eight items that measure: pain (25 points), instability (25 points), locking (15 points), swelling (10 points), limp (5 points), stair climbing (10 points), squatting (5 points), and need for support (5 points). Every question response has been assigned an arbitrary score on an increasing scale. The total score is the sum of each response to the eight questions, and may range from 0-100.

  7. Veterans Rand 12 (VR-12) General Health Survey [pre-operatively and post-operatively at 3 and 6 months]

    VR-12 includes 12 original question items from the VR-36. The questions in this survey correspond to seven different health domains: general health perceptions, physical functioning, role limitations due to physical and emotional problems, bodily pain, energy/fatigue levels, social functioning and mental health. Answers are summarized into two scores, a Physical Component Score (PCS) and a Mental Component Score (MCS) which then provides an important contrast between the respondents' physical and psychological health status. The higher the score, better outcomes

  8. Lower extremity functional scale [pre-operatively and post-operatively at 3 and 6 months]

    Questionnaire containing 20 questions about a person's ability to perform everyday tasks. The LEFS can be used by clinicians as a measure of patients' initial function, ongoing progress and outcome, as well as to set functional goals. The columns on the scale are summed to get a total score. The maximum score is 80. The higher the score, better outcomes = 80/80 =100%

  9. Sports Medicine Questionnaire [pre-operatively and post-operatively at 3 and 6 months]

    Assess return to activity; no scale, individual questions

  10. Patient satisfaction [Post-operatively at 3 and 6 months]

    0- 100, higher the score, the better

Eligibility Criteria

Criteria

Ages Eligible for Study:
14 Years to 70 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Between ages 14-70 years old

  • Has suspected meniscus root tear

  • Able to consent for themselves for adults

  • English speaking

  • Males or females

  • Is willing and able to comply with the clinical trial plan and able to understand and sign the Patient Informed Consent Form.

Exclusion Criteria:
  • < 14 years old or open physes

  • 70 years old

  • Pregnant

  • Previous or concurrent vascular injury (vascular bypass procedure)

  • Associated fractures requiring concurrent surgery

  • Found to have contraindications to MRI based on a systematic safety screening developed by the CMRR

Contacts and Locations

Locations

Site City State Country Postal Code
1 Twin Cities Orthopedics Edina Minnesota United States 55435

Sponsors and Collaborators

  • Twin Cities Orthopedics

Investigators

  • Principal Investigator: Robert F LaPrade, MD, PhD, Twin Cities Orthopedics

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Twin Cities Orthopedics
ClinicalTrials.gov Identifier:
NCT05088525
Other Study ID Numbers:
  • RFL_UMN-7T MRI
First Posted:
Oct 22, 2021
Last Update Posted:
Oct 22, 2021
Last Verified:
Oct 1, 2021
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Twin Cities Orthopedics
Additional relevant MeSH terms:

Study Results

No Results Posted as of Oct 22, 2021