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Search / Trial NCT06906094

Prevention of Post mEniscectomy Osteoarthritis: From New Animal Model to Patient pRofiLing

Launched by ISTITUTO CLINICO HUMANITAS · Mar 25, 2025

Trial Information

Current as of June 26, 2025

Enrolling by invitation

Keywords

Meniscectomy Surgery

ClinConnect Summary

Patient demographic, anamnestic, clinical, radiological and morphological data will be collected and reported in the database PEARL, assigning an individual ID to each patient. The most relevant and abundant miRNAs obtained through the transcriptomic analyses will be included too. Information about age, gender, body mass index, type of meniscal lesion, type of injury (if any), time of symptoms onset, general knee condition, previous surgical and/or pharmacological treatments, co-morbidities will be included too. Subjective knee evaluations of patients will be collected by using internationa...

Gender

ALL

Eligibility criteria

  • Inclusion Criteria:
  • 1. Signed Informed Consent Form;
  • 2. Male or female patients ≥18 years of age at time of screening;
  • 3. Patients physically and mentally able to comply with all aspects of the study, including the requirements for follow-up visits;
  • 4. Patients suffering from symptomatic medial and/or lateral degenerative meniscal lesion identified at MRI with a surgical indication of arthroscopic partial meniscectomy;
  • 5. In case of bilateral degenerative meniscus, patients with no or mild pain in the contralateral knee, defined as a score \< 2 on a 0-10 numerical rating scale (NRS);
  • 6. Patients who, before the last 3 months, have undergone and failed at least one prior conservative OA treatment (NSAIDs, physiotherapy, hydrokinesitherapy);
  • 7. Body mass index (BMI) ≤ 40 kg/m2
  • Exclusion Criteria:
  • 1. Presence of clinically observed active infection in the index knee joint or skin disease/breakdown or infection in the area of the planned injection site of the index knee
  • 2. Patients who experienced traumatic injury at the index knee within 6 months prior to the procedure;
  • 3. Patients with a history of invasive malignancies (except non- melanoma skin cancer), unless treated with curative intent and with no clinical signs or symptoms of the malignancy for 5 years;
  • 4. Patients with known systemic disorders or any systemic inflammatory condition such as rheumatoid arthritis;
  • 5. Patients with known metabolic bone diseases such as those affecting calcium metabolism;
  • 6. Patients with a BMI greater than 40 kg/m2,
  • 7. Patients who abuse of the following substances: alcohol, recreational drugs;
  • 8. Major surgery (e.g. osteotomy) of the index knee within 12 months prior to screening;
  • 9. Minor surgery (e.g. shaving or arthroscopy) of the index knee within 6 months prior to screening;
  • 10. Use of systemic immunosuppressants within 6 weeks prior to screening;
  • 11. Any documented clinically significant degree of cognitive impairment or other condition, finding, or psychiatric illness at screening which, in the opinion of the investigator, could compromise patient safety or interfere with the assessment of the safety and treatment effects of the study injection;

About Istituto Clinico Humanitas

Istituto Clinico Humanitas is a leading clinical research organization based in Italy, dedicated to advancing medical science through innovative clinical trials and research initiatives. With a strong emphasis on patient-centered care and cutting-edge methodologies, the institute collaborates with various stakeholders in the healthcare sector to develop and evaluate new therapies and treatment protocols. Its multidisciplinary team of experts is committed to ensuring the highest standards of ethical practice and scientific rigor, contributing to significant advancements in medical knowledge and improved patient outcomes.

Locations

Milano, Rozzano, Italy

Milan, Milano, Italy

Sassari, , Italy

Patients applied

0 patients applied

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported