CompletedN/Aketamine

Anesthetics in Rhytidoplasty - A Comparison Study

Sponsored by Mercy Facial Plastic Surgery Center

NCT ID
NCT02410460
Target Enrollment
30 participants
Start Date
2013-09
Est. Completion
2014-06

About This Study

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.

Conditions Studied

Rhytidoplasty

Interventions

  • clonidine
  • glycopyrrolate
  • propofol
  • ketamine
  • marcaine
  • scopolamine
  • midazolam
  • ondansetron
  • metoclopramide
  • glycopyrrolate
  • lidocaine
  • famotidine
  • desflurane
  • sevoflurane

Eligibility

Sex:FEMALE
Age:18 Years - N/A
Healthy Volunteers:No
View full eligibility criteria
Inclusion criteria:

* Female
* 18 years of age or older
* Undergoing elective rhytidoplasty

Exclusion criteria:

* Male
* Under 18 years old
* Pregnant or breastfeeding
* Medically unfit to undergo surgery
* Undergoing brow-lift in conjunction with rhytidoplasty (due to the inability to properly secure the BIS monitor as it would lie within the surgical field)

Study Locations (1)

Mercy Facial Plastic Surgery Center
Springfield, Missouri, United States

This trial is not recruiting

This study has completed enrollment. Check back for results or find similar trials.

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Data Source
ClinicalTrials.gov

Last updated from source