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Anesthetics in Rhytidoplasty - A Comparison Study

NCT02410460 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 30

Last updated 2015-04-07

No results posted yet for this study

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.

Conditions

  • Rhytidoplasty

Interventions

DRUG

clonidine

DRUG

glycopyrrolate

DRUG

propofol

DRUG

ketamine

DRUG

marcaine

DRUG

scopolamine

DRUG

midazolam

DEVICE

ondansetron

DRUG

metoclopramide

DRUG

glycopyrrolate

DRUG

lidocaine

DRUG

famotidine

DRUG

desflurane

DRUG

sevoflurane

Sponsors & Collaborators

  • Mercy Facial Plastic Surgery Center

    lead OTHER

Study Design

Allocation
RANDOMIZED
Masking
TRIPLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2013-09-30
Primary Completion
2014-06-30
Completion
2014-06-30

Countries

  • United States

Study Locations

More Related Trials

Entities

Drugs

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02410460 on ClinicalTrials.gov