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NCT00951236 Clinical Trial

Study Comparing One Versus Two Cortisone Injections for Trigger Finger

Trigger Finger Clinical Trial

Official title:
A Prospective, Randomized Study Comparing One vs. Two Cortisone Injections for Trigger Finger

Clinical Trial Details — Status: Recruiting

Administrative data
NCT number NCT00951236
Other study ID # RIUCLEI 09-01
Secondary ID
Status Recruiting
Phase N/A
First received July 31, 2009
Last updated February 10, 2014
Start date May 2009

Study information
Verified date February 2014
Source Rothman Institute Orthopaedics
Contact Charles Leinberry, MD
Phone 267-339-3677
Email charlie.leinberry@rothmaninstitute.com
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Interventional

Clinical Trial Summary

Trigger finger, also known as stenosing tenosynovitis, is a painful condition that can cause discomfort and disability. Many physicians choose to locally inject cortisone into the infected finger although there is no current consensus as to how many injections are needed to achieve maximum relief. This study will be a prospective, randomized study to compare one versus two injections for the treatment of trigger finger.

Recruitment information / eligibility
Status Recruiting
Enrollment 392
Est. completion date
Est. primary completion date
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Subject is greater than 18 years of age, presenting with stenosing tenosynovitis.

- Subject is willing and able to provide informed consent.

Exclusion Criteria:

- Patients who have previously undergone surgery for the treatment of trigger finger.

Study Design

Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Primary Purpose: Treatment

Related Conditions & MeSH terms

Intervention

Drug:
• One cortisone injection
Patients in this arm will receive one cortisone injection for the treatment of his/her symptoms
• Two cortisone Injections
Subjects randomized to this treatment will receive two cortisone injections, 4-6 weeks apart

Locations
Country Name City State
United States Rothman Institute: Egg Harbor Township Location Egg Harbor Township New Jersey
United States Rothman Institute: Manahawkin location Manahawkin New Jersey
United States Rothman Institute: Media location Media Pennsylvania
United States Rothman Institute Center City Location Philadelphia Pennsylvania
United States Rothman Institute, Northeast Philadelphia location Philadelphia Pennsylvania
United States Rothman Institute, South Philadelphia Location Philadelphia Pennsylvania
United States Rothman Institute: Vorhees location Vorhees New Jersey

Sponsors (1)
Lead Sponsor Collaborator
Rothman Institute Orthopaedics

Country where clinical trial is conducted

United States, 

Outcome
Type Measure Description Time frame Safety issue
Primary To determine if there is a difference in the incidence of pain, stiffness, clicking or locking at 6 months following final injection No
Secondary To evaluate treatment response among diabetic patients No
Secondary To evaluate treatment response between thumbs and fingers No
Secondary To evaluate treatment response between nodular versus diffuse tenosynovitis No
See also
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Completed NCT05435950 - Clinical Investigation on Safety, Performance and Effectiveness of Sono-instruments N/A
Completed NCT04900220 - Differences in Flare Reaction Incidence and Intensity Following Trigger Finger Injections Phase 4
Completed NCT06401473 - Using the Gate Control Theory of Pain to Decrease Pain During Trigger Finger Corticosteroid Injections N/A
Completed NCT04354415 - Tourniquet vs. No Tourniquet for Carpal Tunnel and Trigger Finger Release N/A
Recruiting NCT06296017 - Effectiveness of Conservative Interventions in the Treatment of Trigger Finger N/A
Completed NCT06288685 - Percutaneous Trigger Finger Release Concomitant Steroid Injection Versus Percutaneous Trigger Finger Release Alone Phase 3
Completed NCT06382623 - Efficacies of Different Managements in Patients With Trigger Finger
Active, not recruiting NCT04568993 - The TriggerHappy Trial N/A
Completed NCT04023695 - Trigger Finger Corticosteroid Injection With and Without Local Anesthetic Phase 4
Recruiting NCT04645303 - Injection of Hyaluronic Acid Versus Corticosteroid for Treatment of Trigger Finger Early Phase 1
Recruiting NCT03156829 - Effectiveness of Cortisone Injection and Splinting for Trigger Finger Phase 4
Completed NCT01987115 - Comparison of Fascial Manipulation With Traditional Physiotherapy for the Treatment of Trigger Fingers N/A
Completed NCT01950793 - A Comparison Between Sonoguided Injection Corticosteroid and Hyaluronic Acid Injection in Treatment of Trigger Finger N/A
Completed NCT02196233 - Surgical Treatment of Adult Trigger Finger
Recruiting NCT04675892 - Resection of Flexor Digitorum Superficialis Tendon for Severe Trigger Fingers N/A
Terminated NCT05082480 - Evaluate the Effectiveness of Crosslinked HA on the Adhesion Preventing After Trigger Finger Release Surgery N/A
Recruiting NCT05045157 - Effectiveness of Percutaneous Pulley Release With Infiltration, Versus Infiltration Alone in Trigger Finders N/A
Active, not recruiting NCT01886157 - Treatment of Trigger Finger With Steroid Injection Versus Steroid Injection and Splinting N/A
Withdrawn NCT04855942 - Focused Extracorporeal Shock Wave Therapy (ESWT) Versus Traditional Physiotherapy in the Treatment of Trigger Finger N/A