Degenerative Joint Disease Of Knee

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Review clinical trials related to Degenerative Joint Disease Of Knee. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Not yet recruiting

Intra-Articular Adelmidrol 2%/Hyaluronic Acid 1% With or Without m/umPEA, in Knee Pain Due to Joint Degeneration.

Degenerative knee joint diseases are characterized by chronic pain, inflammation, and functional impairment. In these conditions, mast cell density in the synovial membrane is increased, resulting in an excessive release of biological mediators involved in key mechanisms of neuroinflammation and in hyaluronic acid depolymerisation. Adelmidrol acts as a preventive antioxidant due to its radical scavenging activity, thus protecting hyaluronic acid from oxidative degradation and reducing mast cell degranulation. Furthermore, a reduction in endogenous Palmitoylethanolamide (PEA) levels also contributes to joint neuroinflammation and disease progression; therefore, its exogenous supplementation may represent a valuable supportive strategy. The objective of this clinical investigation is to compare the efficacy of intra-articular adelmidrol/hyaluronic acid treatment alone versus the same intra-articular treatment combined with oral micronized /ultramicronized PEA in patients with knee joint degeneration due to osteoarthritis or rheumatoid arthritis.

Participants needed: 80
Trial details
Age: 40+Biological sex: AllType: InterventionalSponsor: Universita di VeronaUpdated: Jul 2, 2026Locations: 1
Eligibility criteria

Age ≥ 40 years [+7]

Severe progressive systemic diseases [+8]

Status: Recruiting

Long-Term Study of CartiPRO for Knee Pain Due to Osteoarthritis or Cartilage Damage

This clinical trial aims to evaluate and compare the efficacy and safety of CartiPRO, an approved intra-articular atelocollagen injection, versus Synovian injection for the relief of knee pain in patients with knee osteoarthritis. The investigational device is administered intra-articularly, with a second injection given 24 weeks after the first dose. Primary and secondary endpoints include changes in pain scores (VAS), functional assessments (WOMAC, SF-36), and safety evaluations over a 36-week period.

Participants needed: 194
Trial details
Age: 19+Biological sex: AllType: InterventionalSponsor: DALIM TISSEN Co., Ltd.Updated: Jan 20, 2026Locations: 5
Eligibility criteria

Age 19 years and older [+11]

Body Mass Index (BMI) ≥32 kg/m² [+34]

Status: Recruiting

Physica System Total Knee Replacement Registry Study

The primary objective of this study is to obtain long-term implant survivorship (out to 10 years) and to assess clinical, patient-reported outcome measures, and radiographic data for the commercially available Physica system. For ancillary arm, from baseline to 5-year follow-up.

Participants needed: 800
Trial details
Age: 22+Biological sex: AllType: InterventionalSponsor: Limacorporate S.p.aUpdated: Mar 21, 2023Locations: 5
Eligibility criteria

Males and females of any race requiring a total knee replacement and suitable fo... [+5]

Patients with severe instability of the knee joint secondary to the absence of c... [+16]