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Clinical Trial Summary

The primary objective of investigators' proposed study is to demonstrate that the following two cohorts undergoing total hip arthroplasty will have equivalent visual analog scale (VAS) scores up to 3 months post-operatively: one that is administered a modified multimodal analgesic pathway without opioids and the other administered the current standard multimodal analgesic pathway used at Johns Hopkins Bayview Hospital (which includes opioids). The secondary objective is to demonstrate that these cohorts will also have equivalent functional outcomes as determined by both objective measures (such as hip range of motion) and patient-reported outcome measures, such as the Hip Disability and Osteoarthritis Outcome Score (HOOS) and the University of California at Los Angeles (UCLA) activity score.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT04421196
Study type Interventional
Source Johns Hopkins University
Contact
Status Withdrawn
Phase N/A
Start date September 15, 2022
Completion date December 1, 2023

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