Evaluation of Meniscal Extrusion by Dynamic Ultrasonography in Patients With Ostearthritis

Sponsor
Istituto Ortopedico Rizzoli (Other)
Overall Status
Recruiting
CT.gov ID
NCT06113536
Collaborator
(none)
202
1
1
33.3
6.1

Study Details

Study Description

Brief Summary

This is a diagnostic, open-label, single-center interventional study. The aim of the study is to evaluate the relationship between medial and lateral meniscus extrusion determined by dynamic ultrasound study and bone edema assessed by MRI study in patients with knee OA.

As a secondary objective, the correlation of the above parameters with the patient's symptomatology assessed by subject clinical questionnaires will be evaluated.

Condition or Disease Intervention/Treatment Phase
  • Diagnostic Test: Ultrasonographic evaluation
N/A

Detailed Description

Patients with a diagnosis of knee OA will be included in a study involving evaluation of the correlation between meniscal extrusion assessed by dynamic ultrasonography and bone edema assessed on MRI. A total of 202 patients will be included, who, after providing their signed informed consent to participate in the study, will undergo dynamic ultrasonography. After giving signed consent to participate in the study, the patient will undergo the following examinations::

  • ultrasound evaluation for assessment of possible meniscal extrusion;

  • At the same time as the ultrasound examination, subjective questionnaires will be administered to patients.Recent radiological examinations of the patients or from the patient's medical record will be collected during or before the diagnostic investigation.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
202 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Intervention Model Description:
This is a diagnostic, open-label, single-center interventional study.This is a diagnostic, open-label, single-center interventional study.
Masking:
None (Open Label)
Primary Purpose:
Diagnostic
Official Title:
Evaluation of Meniscal Extrusion by Dynamic Ultrasonography in Patients With Ostearthritis and Comparison With Magnetic Resonance Imaging Study.
Actual Study Start Date :
Mar 23, 2021
Anticipated Primary Completion Date :
Jan 1, 2024
Anticipated Study Completion Date :
Jan 1, 2024

Arms and Interventions

Arm Intervention/Treatment
Experimental: Ultrasonographic evaluation

Ultrasonographic evaluation for assessment of possible meniscal extrusion

Diagnostic Test: Ultrasonographic evaluation
Ultrasonographic evaluation for assessment of possible meniscal extrusion

Outcome Measures

Primary Outcome Measures

  1. Meniscal extrusion [baseline]

    Meniscal extrusion in clinostatism and orthostatism, assessed in millimeters (mm) or percent meniscal extrusion relative to tibial margin, and difference between the two measurements

Secondary Outcome Measures

  1. IKDC-Subjective Score (Subjective International Knee Documentation Committee) [baseline]

    This is a subjective, knee-specific rating scale that is considered one of the most reliable assessment tools in the evaluation of knee pathology. The questionnaire examines 3 categories: symptoms, sports activity, and knee function

  2. KOOS Score ( Knee Injury and Osteoarthritis Outcome score) [baseline]

    The full questionnaire consists of five subscales and they cover: pain (9 items), symptoms (7 items of which two relate to stiffness), functions and activities of daily living (17 items) physical function, sports activities and leisure (5 items) and quality of life in relation to the knee (4 items). All items in the relevant subscales have the same response mode, use a 5-point Likert scale, and each question is assigned a score from 0 to 4, where 0 indicates "no difficulty" and 4 "a severe difficulty). Score range 0-100 for each subscale

  3. VAS-dolore (Visual Analogue Scale) [baseline]

    Visual analog scale consisting of a straight line segment (10 cm length), the ends of which correspond to "no pain" and "the strongest pain imaginable."

  4. Tegner Activity Level Scale [baseline]

    The Tegner Activity Level Scale: allows the estimation of a subject's motor activity level with a score between 0 and 10, where 0 represents 'inability' and 10 represents 'participation in competitive sports, such as soccer at the national or international level. This score is the one most commonly used to define the motor activity level of patients with knee disorders.

  5. EQ-VAS [baseline]

    Visual analog scale consisting of a straight line segment (10 cm length), the ends of which correspond to "no pain" and "the strongest pain imaginable."

  6. Objective parameters - Circumferences [baseline]

    Bilateral trans- and supra- patellar circumferences measurement for comparative analysis.The measurement will be taken by the orthopedist by meter and will be reported in centimeters

  7. Objective parameters- Range of Motion [baseline]

    Evaluation of the Range of Motion for comparative analysis. Range of motion (ROM) is a term used to describe how far you can move a joint or muscle in various directions. It is used to measure how much you can move a joint on your own (active ROM) or with the assistance of someone else (passive ROM).Range of motion is measured using a goniometer.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 80 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  1. Age between 18 and 80 years;

  2. Signs and symptoms of degenerative pathology of knee cartilage;

  3. Patients with Radiographic (X-ray or MRI) signs of OA (K-L grade 0-4); 3.

  4. Cooperative patients with pain that does not prevent orthostatism

  5. Ability and consent of patients to actively participate in clinical follow-up;

  6. Recently performed MRI (maximum 1 month).

Exclusion Criteria:
  1. Patients unable to express consent;

  2. Patients undergoing intra-articular infiltration of other substance in the previous 6 months;

  3. Patients undergoing knee surgery in the previous 12 months;

  4. Patients with malignant neoplasms;

  5. Patients with rheumatic diseases;

  6. Patients with a history of total/subtotal meniscectomy;

  7. Patients with symptomatology such that a dynamic examination in orthostatism is not possible; 7.

  8. Patients abusing alcoholic beverages, drugs or medications;

  9. Body Mass Index > 40;

  10. Pregnant or lactating women;

  11. Patients with axis deviation > 5°.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Istituto Ortopedico Rizzoli Bologna Italy 40136

Sponsors and Collaborators

  • Istituto Ortopedico Rizzoli

Investigators

  • Principal Investigator: Luca Andriolo, MD, Istituto Ortopedico Rizzoli - II Clinica Ortopedica e Traumatologica

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Istituto Ortopedico Rizzoli
ClinicalTrials.gov Identifier:
NCT06113536
Other Study ID Numbers:
  • US-MEN
First Posted:
Nov 2, 2023
Last Update Posted:
Nov 2, 2023
Last Verified:
Oct 1, 2023
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 Istituto Ortopedico Rizzoli
Additional relevant MeSH terms:

Study Results

No Results Posted as of Nov 2, 2023