The TriggerHappy Trial
Condition(s) studied
Investigational drug(s) / intervention(s)
Proximal phalangeal level: Injection of methyl prednisone and lidocaine in the tendon sheet at the level of the proximal phalanx
Volar to the MCP-joint: Injection of methyl prednisone and lidocaine in the tendon sheet volar to the MCP-joint
Study summary
This is a prospective randomized multicenterstudy focusing on PROMs after primary corticoid injection for triggerfinger with a comparison of two different injection techniques.
Eligibility
Primary outcome measure(s)
- Pain after injection — Four weeks
Visual analouge scale (VAS), range 0-10, where 0 indicates "no pain" and 10 "maximum pain" - Impairment of finger motion — Four weeks
Visual analouge scale (VAS), range 0-10, where 0 indicates "no impairment" and 10 "maximum impairment" - Triggering — Four weeks
Visual analouge scale (VAS), range 0-10, where 0 indicates "no trigger phenomenon" and 10 "Trigger phenomenon all the time/ locked finger"
Trial sites (1)
| Facility | City | Region | Status |
|---|---|---|---|
| Alingsås Lasarett/ District Hospital | Alingsås | Sweden |
More Sahlgrenska University Hospital trials in Sweden
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT04568993 on ClinicalTrials.gov ↗ ← All trials in Sweden