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Clinical Trial Summary

The purpose of this study is to compare the efficacy of Bupivicaine and Lidocaine for postoperative pain control in thyroid surgery.


Clinical Trial Description

Patients planned for total thyroidectomy will be recruited for participation. After being informed about the study and potential risks, all patients giving written informed consent will be screened for eligibility for study entry. Patients that meet inclusion and exclusion criteria will be randomized via block randomization in a double blind fashion and a 1:1 ratio to surgical incision infiltration with Bupivacaine (0.5% with 1:200 000 epinephrine) or Lidocaine (2% with 1:100 000 epinephrine). ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04427904
Study type Interventional
Source St. Joseph's Healthcare Hamilton
Contact Michael Xie, MD
Phone (905) 522-1155
Email michael.xie@medportal.ca
Status Recruiting
Phase Phase 2
Start date June 1, 2022
Completion date December 31, 2025

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