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Corticosteroid
Splint + Cortico-steroid injection for Trigger Finger
Phase 4
Waitlist Available
Led By Ruby Grewal, MD
Research Sponsored by Lawson Health Research Institute
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 1 year
Awards & highlights
Study Summary
This trial is testing the effectiveness of corticosteroid injections, splinting, and a combination of the two to treat trigger finger.
Eligible Conditions
- Trigger Finger
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 1 year
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~1 year
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Resolution of symptoms
Secondary outcome measures
Grip Strength (Affected hand)
Grip Strength (Un-affected hand)
Incidence of Triggering: Number of times finger 'catches' with 10 repeated grip attempts
+7 moreSide effects data
From 2015 Phase 4 trial • 400 Patients • NCT0123853622%
All other self reported adverse events
3%
Hospitalization or Surgery
1%
Dural puncture
100%
80%
60%
40%
20%
0%
Study treatment Arm
Epidural Steroid Injection
Epidural Local Anesthetic Injection
Trial Design
3Treatment groups
Experimental Treatment
Group I: Splint and cortico-steroid combinedExperimental Treatment1 Intervention
Group II: Splint aloneExperimental Treatment1 Intervention
Group III: Cortico-steroid aloneExperimental Treatment1 Intervention
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Betamethasone
FDA approved
Find a Location
Who is running the clinical trial?
Lawson Health Research InstituteLead Sponsor
656 Previous Clinical Trials
413,308 Total Patients Enrolled
Ruby Grewal, MDPrincipal InvestigatorSchulich School of Medicine and Dentistry\Surgery
Frequently Asked Questions
These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.
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