Comparison of Ultrasound-guided Intraarticular Hip Injections With and Without Prior Local Anesthesia: a Randomized Controlled Trial
Trial Snapshot
- Phase
- Not Applicable
- Status
- Completed
- Sponsor
- University of Rochester
- Enrollment
- 42
- Locations
- 2
- Primary Endpoint
- mean pain score
Study Overview
Brief Summary
In this single-center randomized controlled trial, subjects undergoing a first-time ultrasound-guided unilateral intraarticular hip injection will be randomized into one of two groups: hip injection with prior local anesthesia (With LA) or hip injection without prior local anesthesia (Without LA). Visual analog scale (VAS) pain scores (0-100) will be collected after the local anesthesia injection (With LA group) and intraarticular hip injection (both groups). The primary outcome measure for comparison between the two groups will be VAS score for the intraarticular hip injection.
Study Design
- Study Type
- Interventional
- Allocation
- Randomized
- Intervention Model
- Parallel
- Primary Purpose
- Treatment
- Masking
- Single (Care Provider)
Eligibility Criteria
- Ages
- 18 Years to — (Adult, Older Adult)
- Sex
- All
- Accepts Healthy Volunteers
- No
Inclusion Criteria
- •patients undergoing a first-time ultrasound-guided unilateral intraarticular hip injection
- •Subjects must be fluent in English
- •Subject must be able to consent for themselves and mark pain levels on a visual analog scale.
Exclusion Criteria
- •previous intraarticular hip injection (to remove bias from prior injection experiences)
- •prior surgery on the hip to be injected
- •use of opioid medication on the day of or day before the procedure
- •diabetes mellitus
- •body mass index (BMI) greater than 40
Outcomes
Primary Outcomes
mean pain score
Time Frame: baseline
A visual analog pain score will be collected. The scale of the score is 0-100 with 100 indicating more pain.
Secondary Outcomes
No secondary outcomes reported
Investigators
Rondy Lazaro
Assistant Professor
University of Rochester
