Clinical Trials Directory

Trials / Completed

CompletedNCT03358888

Prolonged Multimodal Analgesia for Post-Discharge Pain Control After Primary Total Hip Arthroplasty

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
228 (actual)
Sponsor
Rothman Institute Orthopaedics · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

This is a prospective, three-arm, comparative study with a provider-crossover design. The first arm will comprise the standard of care pain regimen after discharge, which comprises PRN oxycodone, tramadol, and acetaminophen. The second arm will comprise a multimodal pain regimen; however, patients will still be routinely provided PRN oxycodone and tramadol to use on an as needed basis. The third arm will comprise a multimodal pain management protocol, which does not routinely allow for opioid consumption. However, patients will be provided a one week supply of oxycodone and tramadol for emergency pain relief only.

Conditions

Interventions

TypeNameDescription
DRUGMulti-modal with as needed opioidsMulti-modal with as needed oxycodone and tramadol provided for break-through pain
DRUGMulti-modal with one week of opioids offeredMulti-modal with only one week of oxycodone and tramadol provided for emergency pain relief only
DRUGStandard of CareThis arm follows standard of care post-operative pain management with oxycodone, tramadol, and acetametophin

Timeline

Start date
2017-06-05
Primary completion
2018-01-22
Completion
2018-02-28
First posted
2017-12-02
Last updated
2019-01-29

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT03358888. Inclusion in this directory is not an endorsement.