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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT06370312
Other study ID # 2023-07921-01
Secondary ID
Status Not yet recruiting
Phase
First received
Last updated
Start date May 1, 2024
Est. completion date April 30, 2027

Study information

Verified date April 2024
Source Region Skane
Contact Elisabeth Brogren, MD, PhD
Phone +46 40331723
Email elisabeth.brogren@med.lu.se
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The study project aims at examining molecular markers in synovial fluid, bone and articular cartilage from osteoarthritic thumb basal joints. The degradation of extracellular matrix (ECM) proteins in thumb basal joints will be evaluated in association to the metabolic profile of the patient, but we also aim to compare the ECM degradation and inflammatory profiles with articular cartilage degradation ECM profile from knee joints with osteoarthritis. A third aim is to evaluate associations between patient-reported hand function, pain, strength and range of thumb motion to analyses of synovial fluid.


Description:

Patients scheduled for trapeziectomy on the basis of thumb basal joint osteoarthritis will be asked to participate. Synovial fluid from the thumb basal joint is aspirated before the joint is opened. The trapezium bone and cartilage is harvested. Blood samples to evaluated lipid profile and glucose intolerance is drawn. Blood pressure and measurements of obesity is taken. Patients are also examined at baseline and 1 year postop with grip strength, pinch strength, range of thumb motion and asked to fill in patient-rated outcome measures; QuickDASH and NRS pain.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 120
Est. completion date April 30, 2027
Est. primary completion date April 30, 2026
Accepts healthy volunteers No
Gender All
Age group 25 Years and older
Eligibility Inclusion Criteria: - Men and women age = 25 years - Radiologically confirmed and symptomatic thumb basal joint osteoarthritis (OA) planned for trapeziectomy Exclusion Criteria: - Previous surgery to the affected thumb basal joint - Post-traumatic thumb basal joint OA - Rheumatoid arthritis or other chronic inflammatory arthritis, history of psoriasis affecting joints, gout or pseudogout - Ongoing infection in the hand or wrist - Inability to co-operate with the follow-up protocol or to assimilate information about the study protocol (language difficulties, severe psychiatric disorder, cognitive impairment, drug addiction) - Systemic or intra-articular glucocorticoids or intraarticular platelet-rich plasma or hyaluronic acid injections in the affected joint within 3 months prior to enrollment

Study Design


Intervention

Procedure:
Trapeziectomy
Patients scheduled for trapeziectomy due to thumb basal joint osteoarthritis are invited to participate. Synovial fluid is aspirated before the joint is opened. Bone and cartilage are collected. Blood samples are obtained preop. Patients are measured with grip strength, pinch strength, range of thumb motion, body mass index, central obesity and blood pressure.

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Region Skane

Outcome

Type Measure Description Time frame Safety issue
Primary Serum cholesterol levels Blood samples are drawn from the patients and analysed according to Swedish laboratory standards Serum cholesterol levels are drawn at baseline (i.e. the day of surgery)
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