Actively Recruiting

Phase Not Applicable
Age: 18Years - 70Years
All Genders
ID05882591

Posteromedial Tibiofemoral Incongruence (PMTFI) Treatment to Assess Outcomes of Arthroscopic Surgical Technique

Led by Artromedical Konrad Malinowski Clinic · Updated on 2023-05-31

10

Participants Needed

1

Research Sites

52 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This research aims to assess the outcomes of treating Posteromedial Tibiofemoral Incongruence (PMTFI), a condition where decreased curvature in the femoral metaphysis near the medial femoral condyle causes compression of the posterior horn of the medial meniscus (PHMM) during full knee flexion. This can lead to pain, snapping, discomfort, and worsening meniscus degeneration over time, especially during deep knee bending. The study evaluates a published arthroscopic technique designed to correct this incongruence with minimal necessary intervention, confirming the need for repair during surgery. The study involves a single treatment group receiving the PMTFI treatment following the specific published arthroscopic method. This surgical procedure aims to correct the anatomical incongruence that causes PHMM compression, potentially improving symptoms when conservative treatments have failed. There is no placebo or alternate comparison group mentioned. Participants will be monitored for up to 24 months after treatment. Researchers will assess pain presence during full knee flexion at 12 and 24 months, along with functional outcomes using the International Knee Documentation Committee Questionnaire (IKDC) and the Knee injury and Osteoarthritis Outcome Score (KOOS) at the same intervals. The study includes clinical evaluations, imaging confirmation, and arthroscopic assessment, focusing on symptom relief and functional improvement over time.

CONDITIONS

Brief Title

Posteromedial Tibiofemoral Incongruence (PMTFI) Treatment

Who Can Participate

Age: 18Years - 70Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Adults aged 18 to 70 years
  • Experience pain, snapping, or discomfort in the back of the knee during deep knee flexion such as squatting
  • MRI confirms reduced curvature near the medial femoral condyle
  • Arthroscopic confirmation of impingement of the posterior horn of the medial meniscus during full knee flexion
Not Eligible

You will not qualify if you...

  • Active inflammation in the knee
  • Cartilage injuries graded ICRS 3-4
  • Pain, snapping, or discomfort in the back of the knee caused by conditions outside the joint
  • Presence of cyst or avascular changes near the planned surgical area in the femoral metaphysis

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Surgery and Immediate Post-operative Care

Duration - Surgery day and immediate recovery period

Participants undergo the arthroscopic surgical procedure to treat Posteromedial Tibiofemoral Incongruence (PMTFI) and receive immediate post-operative care.

1 surgical visit and post-operative monitoring

Post-operative Follow-up

Duration - Up to 24 months

Participants are monitored for recovery and assessed for pain and function in the knee following surgery.

Visits at 12 and 24 months post-surgery

Trial Site Locations

Total: 1 location

1

Artromedical Orthopaedic Clinic

Bełchatów, Łódź Voivodeship, Poland, 97-400

Actively Recruiting

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Research Team

K

Konrad Malinowski, MD PhD

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

TREATMENT

Number of Arms

1

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