RecruitingNot Applicable

Study Protocol to Evaluate Clinical and Imaging Results of Knee Fresh Osteochondral Allografts

Spain40 participantsStarted 2018-06-06

Plain-language summary

The main objective of this study is to assess the clinical and radiological results after carrying out a transplant of fresh osteochondral allograft in the knee.

Who can participate

Age range15 Years – 50 Years

SexALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: Patients undergoing cartilage repair with fresh osteochondral allograft transplantation for large focal full-thickness chondral and osteochondral defects (\>2 cm2) on the tibial plateau, femoral condyles, trochlea and/or patella Bipolar lesions are included. Exclusion Criteria: * BMI\> 30 kg / m2 * Systemic inflammatory diseases * Inflammatory arthritis * Advanced osteoarthritis * Tricompartmental degenerative process * Active infection * Patients who are unable to provide written informed consent.

What they're measuring

International Knee Documentation Committee (IKDC) Score

Timeframe: 15 months

Kujala Score

Timeframe: 15 months

Western Ontario Meniscal Evaluation Tool (WOMET)

Timeframe: 15 months

Tegner Activity Scale

Timeframe: 15 months

Patient satisfaction

Timeframe: 15 months

OCAMRISS

Timeframe: 15 months

Bone integration

Timeframe: 15 months

Trial details

NCT IDNCT04236492

SponsorFundació Institut de Recerca de l'Hospital de la Santa Creu i Sant Pau

Sponsor typeOTHER

Study typeOBSERVATIONAL

Primary completion2026-03-10

Contact for this trial

Àlex Grau Blanes

+34935537031 agraub@santpau.cat

View on ClinicalTrials.gov More Osteochondral Defect trials