Evaluation of Effectiveness of Combined Intra-articular and Intra-osseus Injection VS a Single Intra-articular Injection of Bone Marrow Concentrate (INTERFACE)
Primary Purpose
Osteoarthritis, Knee
Status
Completed
Phase
Phase 3
Locations
Italy
Study Type
Interventional
Intervention
Bone Marrow Concentrate
Sponsored by
About this trial
This is an interventional treatment trial for Osteoarthritis, Knee focused on measuring Bone Marrow Comcentrate, intra-articular, intra-osseus
Eligibility Criteria
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.
Sites / Locations
- Rizzoli Orthopaedic Institute
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Experimental
Arm Label
Single intra-articular Bone Marrow Concentrate injection
combined Bone Marrow Concentrate injection
Arm Description
Single intra-articular Bone Marrow Concentrate injection in the knee
combined Bone Marrow Concentrate injection (intra-articular and intra-osseus)
Outcomes
Primary Outcome Measures
change of Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC) score trend over time
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 Outcome Measures
IKDC Subjective Knee Evaluation Form (IKDC)
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.
Full Information
NCT ID
NCT03876795
First Posted
March 12, 2019
Last Updated
April 18, 2023
Sponsor
Istituto Ortopedico Rizzoli
1. Study Identification
Unique Protocol Identification Number
NCT03876795
Brief Title
Evaluation of Effectiveness of Combined Intra-articular and Intra-osseus Injection VS a Single Intra-articular Injection of Bone Marrow Concentrate
Acronym
INTERFACE
Official 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
Study Type
Interventional
2. Study Status
Record Verification Date
April 2023
Overall Recruitment Status
Completed
Study Start Date
November 8, 2019 (Actual)
Primary Completion Date
March 1, 2023 (Actual)
Study Completion Date
March 1, 2023 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Istituto Ortopedico Rizzoli
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
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).
Detailed Description
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.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Osteoarthritis, Knee
Keywords
Bone Marrow Comcentrate, intra-articular, intra-osseus
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
ParticipantOutcomes Assessor
Allocation
Randomized
Enrollment
86 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Single intra-articular Bone Marrow Concentrate injection
Arm Type
Active Comparator
Arm Description
Single intra-articular Bone Marrow Concentrate injection in the knee
Arm Title
combined Bone Marrow Concentrate injection
Arm Type
Experimental
Arm Description
combined Bone Marrow Concentrate injection (intra-articular and intra-osseus)
Intervention Type
Biological
Intervention Name(s)
Bone Marrow Concentrate
Intervention Description
Bone Marrow Concentrate injection
Primary Outcome Measure Information:
Title
change of Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC) score trend over time
Description
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.
Time Frame
basal 2,6,12 months after treatment
Secondary Outcome Measure Information:
Title
IKDC Subjective Knee Evaluation Form (IKDC)
Description
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.
Time Frame
2,6,12 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
40 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
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.
Facility Information:
Facility Name
Rizzoli Orthopaedic Institute
City
Bologna
ZIP/Postal Code
40136
Country
Italy
12. IPD Sharing Statement
Plan to Share IPD
No
Learn more about this trial
Evaluation of Effectiveness of Combined Intra-articular and Intra-osseus Injection VS a Single Intra-articular Injection of Bone Marrow Concentrate
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