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NCT Number: NCT03876795

Evaluation of Effectiveness of Combined Intra-articular and Intra-osseus Injection VS a Single Intra-articular Injection of Bone Marrow Concentrate

Osteoarthritis (OA) is one of the most common diseases resulting in large burdens on society.

Among the emerging treatments, Bone Marrow Concentrate (BMC) intra-articular injections are a promising regenerative approach. However, they offer only a temporary benefit since they target synovial and chondral tissues but fail to address the osteochondral interface, which plays a key role in the onset and progression of joint degeneration.

This project will investigate the efficacy of combined BMC injections, targeting both intra-articular tissues and subchondral bone, to treat OA in a Randomized Controlled Trial (RCT).

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Key information

Age range

40 year–70 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 3

Primary location

Rizzoli Orthopaedic Institute

Bologna, 40136, Italy

About this study

The main aim is to evaluate in a RCT the potential of a new combined BMC treatment for OA, through the use of scores for the clinical outcome, the study of imaging and biological samples for tissue regeneration and systemic effects, and the identification of BMC and patient characteristics predictive of better results.

All patients will undergo an arthroscopic procedure to debride degenerated tissues (this can offer a temporary benefit but not long lasting results) before BMC intra-articular injection. Half patients will receive also the injection of BMC at the subchondral level (bone samples obtained to allow BMC placement will be sent to the Lab).

The same minimally invasive incisions will be used for all patients, ensuring patient blinding. Evaluations, performed by medical staff not involved in the treatment to ensure double blinding, will document subjective clinical improvement, functional measurements, biomarker study, and imaging with the use of modern 3TMRI and qCT technology. BMC characterization and patient features will be analysed to identify factors predictive of a better outcome.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Male or female patients, aged between 40 and 70;
  • Arthrosis of the medial compartment (grade 2-3 according to the Kellgren-Lawrence score> 4 months);
  • Failure after at least 6 months of conservative treatment (drug therapy with NSAIDs and painkillers, hyaluronic acid infiltration, corticosteroid infiltration, PRP);
  • Patients' ability and consent to participate in clinical and radiological follow-up;
  • Signature of informed consent.

Exclusion criteria

  • Patients with trauma in the 6 months prior to surgery;
  • Patients with maligncy;
  • Patients suffering from rheumatic diseases;
  • Patients suffering from non-compensated diabetes;
  • Patients suffering from uncompensated thyroid metabolic disorders;
  • Patients abusing alcoholic beverages, drugs or drugs;
  • Patients with axial deviations> 5 °;
  • Body Mass Index> 35;
  • Patients treated with joint infiltrations in the previous 6 months;
  • Patients treated with surgery at the same knee in the previous 12 months.

Treatment and study plan

Bone Marrow Concentrate

Biological

Bone Marrow Concentrate injection

Primary outcomes

  1. change of Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC) score trend over time

    Time frame: basal 2,6,12 months after treatment

    WOMAC is a validated score, designed to highlight the problems of patients with lower limb pathologies, in particular in terms of pain, stiffness and functionality. The score will be completed by the patient, possibly in the presence of an investigator, and simple guidelines for self-compilation will be provided.

Secondary outcomes

  1. IKDC Subjective Knee Evaluation Form (IKDC)

    Time frame: 2,6,12 months

    IKDC is a validated score used in the evaluation of symptoms, function and sport activity in patients suffering of knee diseases, such as meniscal or ligamentous damage, osteoarthritis. The Subjective Knee Form provides the best method of overall assessment of the most significant symptoms and disabilities for a population that has undergone cartilage repair treatments.

Sponsors and collaborators

Lead sponsor

Istituto Ortopedico Rizzoli

Other

Registry information

Official study title

Evaluation of Effectiveness of Combined Intra-articular and Intra-osseus Injection VS a Single Intra-articular Injection of Bone Marrow Concentrate for the Treatment of Osteoarthritis in the Knee. (INTERFACE) Double Blind, Randomized Clinical Trial

Acronym: INTERFACE

Important dates

Study start
2019
Primary completion
2023
Study completion
2023
First posted
Mar 15, 2019
Registry last updated
Apr 19, 2023

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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