Synovial Fluid Analysis in Arthritic vs Non-arthritic Joints

Overview

About this study

The primary objective of this study is to evaluate biomarkers using ELISA testong of synovial fluid from arthrtiic vs non arthritic knees. Synovial fluid samples collected in this study will be compared to synvial fluid samples from IRB 20-009091

Participation eligibility

Participant eligibility includes age, gender, type and stage of disease, and previous treatments or health concerns. Guidelines differ from study to study, and identify who can or cannot participate. There is no guarantee that every individual who qualifies and wants to participate in a trial will be enrolled. Contact the study team to discuss study eligibility and potential participation.

 Inclusion Criteria:

  • Men and women between the ages of 18-100.
  • Non-arthritic or mildly arthritic knee joints.

Exclusion Criteria:

  • Congenital malformation of the target knee resulting in significant deformity.
  • Surgery on the index knee within 1 year of study enrollment.
  • Injections of any into the index knee within 3 months prior to study enrollment.
  • History of superficial infection in the index knee within 6 months of study enrollment, or evidence of current superficial infection affecting the index knee.
  • Body mass index (BMI) > 40 kg/m^2.
  • Taking anticoagulant medications (e.g., warfarin, heparin) or clopidogrel (Plavix).
  • Taking anti-rheumatic disease medication (including methotrexate or other antimetabolites) within 3 months prior to study enrollment.
  • On chronic, immunosuppressive transplant therapy or having a chronic, immunosuppressive state, including use of systemic steroids/corticosteroids.
  • Systemic inflammatory, rheumatological or connective tissue disorder including but not   limited to rheumatoid arthritis, systemic sclerosis, system lupus erythematosus, and Ehlers-Danlos Syndrome.
  • Rheumatological or inflammatory disease of the knee or chondrocalcinosis/calcium pyrophosphate disease (CPPD), hemochromatosis, inflammatory arthritis, arthropathy of the knee associated with juxta-articular Paget’s disease of the femur or tibia, ochronosis, hemophilic arthropathy, infectious arthritis, Charcot’s knee joint, villonodular synovitis, and synovial chondromatosis.
  • Ongoing infectious disease, including but not limited to tuberculosis, HIV, hepatitis, and syphilis.
  • History of cancer/malignancy with the exception of adequately treated basal cell or squamous cell carcinoma of the skin not associated with the target knee within the last 5 years.
  • History of blood dyscrasia, including but not limited to anemia, thrombocytopenia, and monoclonal gammopathy.
  • Known allergy to local anesthetics of other components of the study drug.
  • History of or current evidence of alcohol or drug abuse or dependence, recreational use of illicit drug or prescription medications, or have use of medical marijuana within 30 days of study entry.
  • Any illness or condition which, in the investigators’ judgement will interfere with the interpretation of the study results.

Eligibility last updated 10/1/21. Questions regarding updates should be directed to the study team contact.

Participating Mayo Clinic locations

Study statuses change often. Please contact the study team for the most up-to-date information regarding possible participation.

Mayo Clinic Location Status Contact

Jacksonville, Fla.

Mayo Clinic principal investigator

Shane Shapiro, M.D.

Open for enrollment

Contact information:

Shaimaa Hassoun M.B., B.Ch., M.D.

(507) 422-5830

Hassoun.Shaimaa@mayo.edu

More information

Publications

Publications are currently not available
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CLS-20546032

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