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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT02684864
Other study ID # PID 11499
Secondary ID
Status Active, not recruiting
Phase
First received
Last updated
Start date March 2016
Est. completion date February 2026

Study information

Verified date November 2020
Source University of Oxford
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Adults with degenerative meniscal tear receiving arthroscopic surgical management or knee drainage (arthrocentesis) +/- intra-articular steroid injection will be recruited to this non-interventional cohort study. The aim is to investigate whether measurement of an individual's synovial fluid biomarker response to a degenerative meniscal tear with symptoms predicts symptomatic and functional outcome suggestive of osteoarthritis (OA) of the knee.


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 150
Est. completion date February 2026
Est. primary completion date February 2023
Accepts healthy volunteers No
Gender All
Age group 30 Years to 60 Years
Eligibility Inclusion Criteria: 1. Male or female aged 30-60 years. 2. Participant able and willing to give informed consent. 3. Clinical assessment demonstrates mechanical symptoms suggestive of meniscal pathology (focal knee pain +/- 1 or more of: catching/locking, giving way, focal joint-line tenderness, effusion, McMurray's positive) within last 12 months. 4. Evidence on clinical MRI knee of meniscal tear. 5. Participant is either in secondary care or has the potential to be referred to secondary care due to severity of symptoms. 6. Patient has failed conservative therapy and elected for surgical arthroscopic treatment, or is due knee drainage/injection for clinical reasons. 7. Competency of the English language to complete questionnaires independently. Exclusion Criteria: 1. Pre-existing advanced radiographic OA (KL grade 3-4) of index knee at baseline. 2. Evidence of anterior cruciate ligament rupture, or more extensive soft tissue injury. 3. History of an acute knee injury (within 12 weeks), or acutely locked knee 4. Known history of inflammatory/septic arthritis of index knee. 5. Knee replacement or other non-arthroscopic knee surgery (e.g. high tibial osteotomy) - previous or planned within 1 year of study start. 6. Index knee surgery within last 3 months, including meniscectomy. 7. Steroid injection to index knee in last 3 months. 8. Active other (treated) inflammatory disease or infection. 9. Positive pregnancy test. 10. Unable to provide blood samples. 11. Unable to give informed written consent.

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Non-interventional


Locations

Country Name City State
United Kingdom Kennedy Insitute of Rheumatololgy, NDORMS, University of Oxford Oxford Oxfordshire

Sponsors (2)

Lead Sponsor Collaborator
University of Oxford Oxford University Hospitals NHS Trust

Country where clinical trial is conducted

United Kingdom, 

Outcome

Type Measure Description Time frame Safety issue
Primary Knee Injury and Osteoarthritis Outcomes Score (KOOS)-4 summary score from validated KOOS questionnaire. To investigate whether measurement of an individual's synovial fluid biomarker response to a degenerative meniscal tear with symptoms predicts symptomatic and functional outcome suggestive of OA of the knee. 2 years
Secondary X ray Kellgren Lawrence (KL) change X ray of knee.Change in KL grade over time will be measured. 2 years
Secondary MRI semi-quantitative score MRI knee. Change in semi-quantitative score over time will be measured. 2 years
Secondary Oxford Knee Score - Activity and Participation Questionnaire (OKS-APQ) The OKS-APQ will be used to document pain and symptoms, and compared with KOOS. 2 years
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