Actively Recruiting
Analysis of Synovial Fluid, Bone and Articular Cartilage From Osteoarthritic Thumb Basal Joints in Relation to Metabolic Risk Factors and Hand Function
Led by Region Skane · Updated on 2025-06-25
120
Participants Needed
2
Research Sites
52 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
This research focuses on patients with osteoarthritis in the thumb basal joint who are scheduled for trapeziectomy surgery. The study aims to examine molecular markers in the synovial fluid, bone, and cartilage from these osteoarthritic joints. It also investigates the breakdown of extracellular matrix proteins in the thumb basal joints and compares these findings with similar degradations in knee joints affected by osteoarthritis. Additionally, the study explores links between the metabolic profile of patients and joint degradation, along with patient-reported hand function, pain, strength, and thumb motion range. During the study, synovial fluid is collected from the thumb basal joint before surgery, and bone and cartilage samples are harvested during the operation. Blood samples are taken to assess lipid profiles and glucose intolerance. Participants undergo measurements of blood pressure, obesity, grip strength, pinch strength, and thumb range of motion. These assessments occur at the start of the study and one year after surgery. Patients also complete questionnaires about hand function and pain levels. Participants are involved in physical examinations and provide biological samples for analysis. Researchers measure serum cholesterol levels at baseline and evaluate patient-reported outcomes using the QuickDASH and numeric rating scale for pain. The study monitors changes in hand strength, motion, and symptoms over time, emphasizing the relationship between metabolic factors and joint health. The overall study duration includes baseline evaluations and a follow-up one year after surgery to assess recovery and joint function.
CONDITIONS
Brief Title
Analysis of Articular Biomarkers From Osteoarthritic Thumb Basal Joints
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Men and women age 65 years or older
- Radiologically confirmed and symptomatic thumb basal joint osteoarthritis planned for trapeziectomy
You will not qualify if you...
- Previous surgery to the affected thumb basal joint
- Post-traumatic thumb basal joint osteoarthritis
- Rheumatoid arthritis or other chronic inflammatory arthritis, history of psoriasis affecting joints, gout or pseudogout
- Ongoing infection in the hand or wrist
- Inability to cooperate with the follow-up protocol or understand study information due to language difficulties, severe psychiatric disorder, cognitive impairment, or drug addiction
- Use of systemic or intra-articular glucocorticoids, platelet-rich plasma, or hyaluronic acid injections in the affected joint within 3 months prior to enrollment
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - Day of surgery
Participants scheduled for trapeziectomy have synovial fluid aspirated before the joint is opened. Bone and cartilage from the trapezium are collected during surgery. Blood samples are drawn to evaluate lipid profile and glucose intolerance. Blood pressure and obesity measurements are taken.
1 visit (in-person)
Duration - 1 year
Participants are examined at baseline and 1 year after surgery with assessments including grip strength, pinch strength, range of thumb motion, and patient-rated outcome measures such as QuickDASH and NRS pain.
2 visits (in-person)
Trial Site Locations
Total: 2 locations
1
Department of Hand Surgery, Skane University Hospital
Malmö, Skåne County, Sweden, 20502
Not Yet Recruiting
2
Aleris Specialistläkare Hyllie
Malmö, Skåne County, Sweden, 21532
Actively Recruiting
Research Team
E
Elisabeth Brogren, MD, PhD
M
My von Walter, MD
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
0
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