Conservative Treatment of Trigger Finger

NARecruitingINTERVENTIONAL
Enrollment

146

Participants

Timeline

Start Date

August 1, 2023

Primary Completion Date

December 31, 2025

Study Completion Date

December 31, 2025

Conditions
Hand InjuriesTrigger Finger
Interventions
DEVICE

Oval-8 ® Orthosis

The experimental group will consist of receiving a PIP joint on the day they receive their cortisone injection. The Oval-8 ® will be issued to the subject by an Occupational Therapist to ensure correct fit and comfort as well as given written instructions for night use. The orthosis will be worn at night for 6-week duration. Participants will have 1 follow up phone call or email at the 6-week mark and then 1 follow up phone call or email at the 12 week mark by a member of the research team from the time they received their cortisone injection where the time for resolution of trigger finger symptoms, VAS (Visual Analogue Scale), subjective questionnaire and QuickDASH scores will all be recorded in their medical research file.

OTHER

Cortisone injection only

The control group will receive a cortisone injection and be instructed to move their fingers normally

Trial Locations (1)

90048

RECRUITING

Cedars-Sinai Medical Center Outpatient Rehabilitation Hand Clinic, Los Angeles

All Listed Sponsors
lead

Cedars-Sinai Medical Center

OTHER