RecruitingNot Applicable

Conservative Treatment of Trigger Finger

United States146 participantsStarted 2023-08-01

Plain-language summary

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.

Who can participate

Age range18 Years – 100 Years

SexALL

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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

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

What they're measuring

Resolution of Trigger Finger Symptoms

Timeframe: 6 Weeks

Resolution of Trigger Finger Symptoms

Timeframe: 12 Weeks

Trial details

NCT IDNCT05837286

SponsorCedars-Sinai Medical Center

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2026-05-31

Contact for this trial

Theodore Brown, BS

800-700-6424 Theodore.Brown@cshs.org

View on ClinicalTrials.gov More Hand Injuries trials