Actively Recruiting
Quantitative Assessment of BB-02 Therapy Effect on Cartilage Status in Patients Affected by Early Knee Osteoarthritis
Led by Istituto Ortopedico Rizzoli · Updated on 2025-07-11
30
Participants Needed
1
Research Sites
103 weeks
Total Duration
On this page
Sponsors
I
Istituto Ortopedico Rizzoli
Lead Sponsor
I
I.R.C.C.S Ospedale Galeazzi-Sant'Ambrogio
Collaborating Sponsor
AI-Summary
What this Trial Is About
Knee osteoarthritis is a condition that affects young or middle-aged patients with high functional demands. Knee replacement surgery in patients under 65 years of age is associated with a high risk of failure and the need for revision. For this reason, it becomes crucial to identify treatment alternatives aimed primarily at resolving symptoms but also at slowing down the joint degenerative process, with the goal of delaying the need for prosthetic treatment as much as possible. The medical device BB-02 (IGEA SpA, Carpi, Italy) is a certified medical device according to Regulation (EU) 2017/745 (MDR) for the treatment of inflammatory and degenerative tissue pathologies and represents an effective tool in the treatment of early and intermediate osteoarthritis. To date, the demonstration of the efficacy of BB-02 therapy has been measured through the evaluation of clinical endpoints, using both objective and subjective assessment scales. So far, there is a lack of instrumental measurement of the ability of BB-02 therapy to preserve the integrity of the articular cartilage. The primary objective of the study is to evaluate, through magnetic resonance imaging (MRI), the effect of pulsed electromagnetic fields administered via BB-02 therapy on cartilage damage in subjects with early-stage osteoarthritis. The BB-02 device was chosen based on promising results reported in the pre-clinical phase of experimentation. The secondary objective is to assess the effect of BB-02 therapy on pain resolution and clinical scores of knee functionality in the two different therapeutic regimens.
CONDITIONS
Official Title
Quantitative Assessment of BB-02 Therapy Effect on Cartilage Status in Patients Affected by Early Knee Osteoarthritis
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Both sexes aged between 20 and 55 years
- Body Mass Index (BMI) less than 35
- Diagnosed with Kellgren-Lawrence grade 2 osteoarthritis
- Baseline Visual Analog Scale (VAS) score of 2 or higher
- Mechanical knee alignment between 175° and 185°
- No acute ligamentous or meniscal knee injuries
You will not qualify if you...
- Presence of systemic inflammatory or cancerous diseases
- Current smoker
- Diagnosis of hypertension or diabetes
- Knee arthroscopy within 12 months before enrollment
- Diagnosed with inflammatory arthritis such as rheumatoid arthritis, gout, joint infections, Lyme disease, or lupus
- Diagnosed with secondary arthritis including acromegaly, Charcot arthropathy, hemochromatosis, Wilson's disease, ochronosis, or anterior cruciate ligament injuries
- Receiving opioid pain medication, systemic corticosteroids, or intra-articular corticosteroids during the study
- Receiving intra-articular hyaluronic acid injections during the study
- Unable to provide informed consent
- Pregnant or breastfeeding women
- Women who are in menopause
AI-Screening
AI-Powered Screening
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Trial Site Locations
Total: 1 location
1
Istituto Ortopedico Rizzoli
Bologna, Italy, 40136
Actively Recruiting
Research Team
S
Stefano Zaffagnini, Professor
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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