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Clinical Trials/NCT05209399
NCT05209399CompletedNot Applicable

Comparison of Ultrasound-guided Intraarticular Hip Injections With and Without Prior Local Anesthesia: a Randomized Controlled Trial

University of Rochester2 sites in 1 country42 target enrollmentStarted: June 30, 2022Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Completed
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

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Rondy Lazaro

Assistant Professor

University of Rochester

Study Sites (2)

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