Prevalence and pattern of radiographic hand osteoarthritis and association with pain and disability (the Rotterdam study).
S Dahaghin, S M A Bierma-Zeinstra, A Z Ginai...
https://pubmed.ncbi.nlm.nih.gov/15374852Actively Recruiting
Led by Université du Québec à Trois-Rivières · Updated on 2026-01-22
40
Participants Needed
2
Research Sites
52 weeks
Total Duration
U
Université du Québec à Trois-Rivières
Lead Sponsor
C
Centre de Recherche de l'Institut Universitaire de Geriatrie de Montreal
Collaborating Sponsor
Researchers are evaluating treatments for trapeziometacarpal osteoarthritis (TMO), a common and painful form of hand arthritis that limits thumb movement and hand function, negatively impacting quality of life. This study aims to compare the effects of saline injections versus corticosteroid injections in reducing pain and improving hand use in people with TMO. This is a double-blind, randomized pilot trial preparing for a larger study, designed to gather initial data on treatment effectiveness and study feasibility. Participants will receive one of two treatments: a single ultrasound-guided injection of either 0.25 ml of saline solution or 0.25 ml (10 mg) of triamcinolone acetonide corticosteroid into the affected joint. The injection procedure is done with imaging guidance to ensure accuracy. The study will last about one year, with recruitment and data collection during this time, focusing on treatment adherence and the success of blinding for both patients and clinicians. During the trial, participants will have their pain levels and hand function assessed at the start and at 1, 3, and 6 months after the injection using numeric pain scales and the QuickDASH questionnaire. Researchers will also monitor analgesic use and any side effects up to six months post-injection. The study will measure recruitment rates, follow-up completion, and how well the blinding was maintained shortly after treatment and during follow-ups.
CONDITIONS
Corticosteroid Against Saline Injections for Thumb Osteoarthritis (CASITOA)
You may qualify if you...
You will not qualify if you...
Complete this quick 3-step screening to check your eligibility
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - Single day
Participants receive a single ultrasound-guided injection of either corticosteroid or saline solution into the thumb joint to treat osteoarthritis.
1 treatment visit (in-person)
Duration - 6 months
Participants are monitored for pain intensity, hand function, medication use, and any adverse events after the injection.
Visits at 1, 3, and 6 months post-injection (in-person or remote)
Total: 2 locations
1
Centre Hospitalier de l'Université de Montréal - Physiatry
Montreal, Quebec, Canada, H2W 1T6
Actively Recruiting
2
Centre Hospitalier de l'Université de Montréal - Chirurgie plastique
Montreal, Quebec, Canada, H2X 0C1
Actively Recruiting
T
Tokiko Hamasaki, PhD
C
Carlos Gevers-Montoro, PhD
Study Type
INTERVENTIONAL
Masking
DOUBLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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