Phase
Condition
Knee Injuries
Osteoarthritis
Treatment
N/AClinical Study ID
Ages 45-85 All Genders
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
Patients suffered from chronic unilateral knee pain for more than 4 months and withroentgenogram degenerative findings of grades 3 and 4 on the Kellgren-LawrenceClassification of Osteoarthritis scale (meaning moderate to severe degrees of knee OA)will be recruited.
The volume of the SF in the supra-patellar bursa region is enough (at least 2 mmthickness in bursa fluid as measured by ultrasound) to be aspirated via ultrasoundguidance.
Small volume of SF will be aspirated first and sent for SF analysis. SF showingevidences of crystals suggesting possible gouty arthritis and infection will not beincluded in this study.
Patient has previously received oral NSAIDs and physical modality treatments butWITHOUT any obvious improvements in knee pain and function. The usage of musculoskeletal ultrasound to confirm that the supra-patellar bursa is incommunication with the synovial cavity of the knee joint. This is to prevent the aspirationof isolated cystic lesion at the supra-patellar region.
Exclusion
Exclusion Criteria:
Total obliteration of knee joint as shown on the roentgenogram images. Patient hassystemic disorders such as diabetes, rheumatoid arthritis, major axial deviation ofthe knee joint (varus >5°, valgus >5°), hematological diseases (coagulopathy), severecardiovascular diseases, infections, and immune-depression.
Patients in therapy with anticoagulants, and taking NSAIDs within the 5 days beforeblood harvest
Patients with hemoglobin value of less than 11 g/dl, and platelet counts of less than 150,000/mm3.
Study Design
Study Description
Connect with a study center
Chang Gung Memorial Hospital
Taoyuan, 33343
TaiwanActive - Recruiting

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