Lidocaine, Esmolol, or Placebo to Relieve IV Propofol Pain

Status Terminated

Clinical Trial Summary

The primary hypothesis is that esmolol and lidocaine, when given without the use of a tourniquet, provide relief of propofol injection pain that is superior to placebo when assessed using the propofol pain scoring tool

Clinical Trial Description

The study will include three arms: lidocaine, esmolol, and placebo. Eligible patients will be 18-60 years old, ASA physical status 1-3, and scheduled for an elective surgical procedure. Patients will be randomized to receive lidocaine, esmolol, or placebo. Both the patients and the administering/observing providers will be blinded to the study drug or placebo being administered ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT04356352
Study type	Interventional
Source	Wake Forest University Health Sciences
Contact
Status	Terminated
Phase	Phase 2/Phase 3
Start date	September 9, 2020
Completion date	August 25, 2023

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