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RECRUITING
NCT05837286
NA

Conservative Treatment of Trigger Finger

Sponsor: Cedars-Sinai Medical Center

View on ClinicalTrials.gov

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.

Official title: Conservative Treatment of Trigger Finger: Outcomes of a Randomized Controlled Trial

Key Details

Gender

All

Age Range

18 Years - 100 Years

Study Type

INTERVENTIONAL

Enrollment

146

Start Date

2023-08-01

Completion Date

2026-05-31

Last Updated

2026-03-27

Healthy Volunteers

No

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

Locations (2)

Cedars-Sinai Medical Center Outpatient Rehabilitation Hand Clinic

Los Angeles, California, United States

Cedars-Sinai Medical Center

Los Angeles, California, United States