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Conservative Treatment of Trigger Finger
Conservative Treatment of Trigger Finger: Outcomes of a Randomized Controlled Trial
Who can join
Ages 18 to 100 · All sexes
Full eligibility criteria
Inclusion Criteria: * Individuals 18 years old or older are included * Patients with trigger finger, aka stenosing flexor tenosynovitis * Status post receiving cortisone injection of the affected digit(s) Exclusion Criteria: * 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
About the study
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.
What is being tested
- Oval-8 ® Orthosis (device)
- Cortisone injection only (other)
Sponsor: Cedars-Sinai Medical Center · Participants: 146 · Started: Aug 1, 2023
Contact the study team
- Theodore Brown, BS · Phone: 800-700-6424
Official record on ClinicalTrials.gov — NCT05837286
Locations in the U.S.
| California | Cedars-Sinai Medical Center, Los Angeles |
Conditions
From ClinicalTrials.gov, data retrieved Sep 30, 2026. Each study sets its own eligibility; the study team decides who can join.