Actively Recruiting
Conservative Treatment of Trigger Finger
Led by Cedars-Sinai Medical Center · Updated on 2026-03-27
146
Participants Needed
2
Research Sites
147 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
This study is to analyze the effectiveness of a nighttime extension orthosis after receiving a cortisone injection for the treatment of trigger finger to improve pain and restore functional outcomes. The investigators hypothesize that the extension orthosis will improve pain and functional outcomes compared to those without a digital night extension orthosis in those with trigger finger at 12 weeks from the injection.
CONDITIONS
Official Title
Conservative Treatment of Trigger Finger
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Individuals 18 years old or older
- Patients with trigger finger, aka stenosing flexor tenosynovitis
- Status post receiving cortisone injection of the affected digit(s)
You will not qualify if you...
- Any records flagged with break the glass or research opt out
- Patients with rheumatoid arthritis
- Patients with a history of traumatic injury to the hand
- Cognitive or behavioral problems which would preclude informed consent
- Unable to speak and understand English
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 2 locations
1
Cedars-Sinai Medical Center Outpatient Rehabilitation Hand Clinic
Los Angeles, California, United States, 90048
Completed
2
Cedars-Sinai Medical Center
Los Angeles, California, United States, 90048
Actively Recruiting
Research Team
T
Theodore Brown, BS
CONTACT
M
Meghan McCullough, MD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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