drugset / Trial / NCT02410460

Anesthetics in Rhytidoplasty - A Comparison Study

NCT02410460

Completed 30 enrolled Mercy Facial Plastic Surgery Center
RandomizedParallel-groupTriple-blind

Summary

This study is a prospective, double-blind, randomized comparison study of different anesthesia methods in rhytidoplasty surgery. The study is designed to determine whether post-operative side-effect profiles in patients undergoing elective cosmetic facelift surgery can be decreased through the use of propofol/ketamine anesthesia with bispectral monitoring (PKA-BIS) rather than general anesthesia, without increasing intra-operative time, side-effect profiles, or patient recall. Approximately 30 subjects undergoing facelift surgery performed by the principal investigator will participate.

Timeline

Start
2013-09
Primary completion
2014-06
Completion
2014-06

Drugs

EvaluationDrugModalityDoseRoute
Subject Desflurane Other / unclassified Inhaled
Subject Ketamine Small molecule 50 mg Intravenous
Subject Ketamine Small molecule 200 mg Intravenous
Subject Propofol Small molecule Intravenous
Subject Sevoflurane Other / unclassified Inhaled
Background Bupivacaine Other / unclassified
Background Clonidine Other / unclassified 0.1 mg
Background Clonidine Other / unclassified 0.2 mg
Background Famotidine Other / unclassified 20 mg
Background Glycopyrrolate Small molecule 0.2 mg
Background Lidocaine Other / unclassified
Background Metoclopramide Small molecule 10 mg
Background Midazolam Small molecule 2 mg
Background Scopolamine Unknown 1.5 mg Other

Indications

No indication recorded.