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Pain After Preoperative UltraSound Guided Hip Injections for Total Hip Arthroplasty (PUSH) — PUSH  

Arthroplasty Clinical Trial

Official title:
Pain After Preoperative UltraSound Guided Hip Injections for Total Hip Arthroplasty (PUSH)

Clinical Trial Summary

The purpose of the study is to assess the accuracy of Butterfly IQ ultrasound for intra-articular hip injections, and to see if an injection given intra-articular before incision provides any benefit in preemptive pain relief or blood loss reduction.

Clinical Trial Description

This study is designed to be prospective randomized (1:1) controlled independent trial. Subjects are male and female, aged 18 and above, who are suitable candidates for either a unilateral (i.e. single) total hip replacement. Subjects that are scheduled with a single, extensively trained Physician Assistant assisting in their surgery will be exclusively included. This is single site study with projected enrollment of 150 subjects ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04219098
Study type Interventional
Source Anne Arundel Health System Research Institute
Contact
Status Not yet recruiting
Phase N/A
Start date February 1, 2020
Completion date August 30, 2020
View Details
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