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Clinical and Instrumental Assessment of Meniscal ROOT Tears Treated Through Suture to the Posterior Cruciate Ligament (ROOT-PCL)

I

Istituto Ortopedico Rizzoli

Status

Enrolling

Conditions

Knee Injuries
Meniscus Tear
Meniscus Lesion

Study type

Observational

Funder types

Other

Identifiers

NCT06507241
ROOT-PCL

Details and patient eligibility

About

The menisci are crucial for knee stability and functionality. Composed of fibrocartilaginous structure, they have an anatomical and biomechanical arrangement that makes them essential for load transmission and the prevention of osteoarthritis. Meniscal root lesions, known as "ROOT tears," compromise their protective function on the cartilage, leading to increased contact pressures between the tibia and femur and, over time, the development of osteoarthritis. Early diagnosis of these lesions is difficult and often the first detection is incidental. The subsequent challenges are significant due to a lack of pre-operative planning. A possible solution is a surgical technique involving arthroscopic suture of the posterior meniscal root along with the posterior cruciate ligament. This procedure does not require pre-operative planning and is applicable even in cases of incidental diagnosis.

Enrollment

59 estimated patients

Sex

All

Ages

18 to 50 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. Age between 18 and 50 years at the time of surgery;
  2. Male and female gender;
  3. Patients undergoing surgical treatment for at least one year for "ROOT" type meniscal lesions using arthroscopic suturing to the posterior cruciate ligament;
  4. Pre-operative MRI performed.

Exclusion criteria

  1. Patients no longer reachable;
  2. Patients who refuse consent to the study;
  3. Previous meniscectomy before surgery;
  4. Previous ligament injuries before surgery;
  5. New traumatic injuries after surgery;
  6. Advanced knee osteoarthritis (Outerbridge grade III-IV) at the time of surgery;
  7. Severe knee malalignment (> 5°) at the time of surgery;
  8. Severe obesity (BMI > 35);
  9. Lower limb conditions preventing full weight-bearing during evaluation;
  10. Infection or hematological/rheumatic conditions at the time of evaluation.

Trial contacts and locations

1

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Central trial contact

Stefano Zaffagnini

Data sourced from clinicaltrials.gov

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