Comparison of ultrasound-guided versus blinded intra-articular lidocaine injection for pain control in reduction of anterior shoulder dislocation: a prospective randomized controlled trial
Phase 3
Completed
- Conditions
- Anterior shoulder dislocationsuccess rate, pain score, Stimson Method, anterior shoulder dislocation, intra-articular lidocaine injection
- Registration Number
- TCTR20210923002
- Lead Sponsor
- Research Faculty of Medicine
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- All
- Target Recruitment
- 28
Inclusion Criteria
age 18-70 years old
Patient with anterior shoulder dislocation
Exclusion Criteria
- Patient who need surgery (anterior shoulder dislocation with associate fracture, open fracture)
- Allergy to lidocaine
- Multiple trauma
- Patient who can't place in prone position
- Do not give consent
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method pain score before the lidocaine injection, after the lidocaine injection, after the shoulder reduction visual analog score , Wonk-Baker FACES pain rating scale
- Secondary Outcome Measures
Name Time Method Success rate After shoulder reduction Physical examination and plain film ,Patient Satisfaction after lidocaine injection, after shoulder reduction Subjective satisfaction scale,Duration at the emergency department the first visit record the time when the patient walk into the ER and discharge from the ER,Complication rate after the shoulder reduction in first visit and 2 weeks after reduction physical examination and plain film