Clinical Trials Directory

Trials / Completed

CompletedNCT05974501

Pre vs Post Block in Total Knee Arthroplasty (TKA)

Pre vs. Postoperative Adductor Canal Block for Total Knee Arthroplasty: Prospective Randomized Trial

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
84 (actual)
Sponsor
University of Miami · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The purpose of this project is to determine if a change in patient reported pain, nausea and vomiting after total knee arthroplasty can be observed with the substitution of a post operative adductor canal block for a preoperative adductor canal block in the current established peri-operative pain protocol and if these changes lead to a decrease in opioid consumption (in morphine equivalents).

Conditions

Interventions

TypeNameDescription
DRUGDexamethasoneDexamethasone 10mg administered via IV once postoperatively within 24 hours for pain and swelling
DRUGAcetaminophen1,000mg administered via tablet every 8 hours for pain during the first 1-2 weeks postoperatively
DRUGLyricaAdministered via tablet 75mg nightly for pain during the first 1-2 weeks postoperatively
DRUGCelebrex200mg administered via tablet twice a day for pain and swelling during the first 1-2 weeks postoperatively
DRUGMeloxicam30mg administered via IV once postoperatively within 24 hours for pain and swelling
DRUGOxycodone5mg administered via tablet every 4 hours as needed for pain during the first 1-2 weeks postoperatively
DRUGRopivacaine20 milliliters Ropivacaine 0.2% administered via injection perioperatively.

Timeline

Start date
2023-09-29
Primary completion
2024-01-22
Completion
2024-01-22
First posted
2023-08-03
Last updated
2025-02-12
Results posted
2025-02-12

Locations

1 site across 1 country: United States

Regulatory

Source: ClinicalTrials.gov record NCT05974501. Inclusion in this directory is not an endorsement.