TerminatedPhase 4ketamine

Delirium Prevention With Ketamine in Ear, Nose, and Throat (ENT) Patients

Sponsored by Emory University

NCT ID
NCT03040024
Target Enrollment
71 participants
Start Date
2017-03-17
Est. Completion
2020-04-24

About This Study

The goal of this prospective randomized double blinded placebo controlled study is to investigate if a single dose of ketamine in addition to standard anesthesia will reduce the risk of delirium in otolaryngeal cancer patients postoperatively. Ketamine's effect on post-operative pain and opioid use will be measured as well. Electroencephalogram (EEG) will be utilized during the surgical procedure to evaluate its potential as a possible predictive device for delirium.

Conditions Studied

Otolaryngeal Cancer

Interventions

  • Ketamine
  • Placebo
  • Electroencephalogram (EEG)

Eligibility

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

* Current diagnosis of otolaryngeal cancer and undergoing surgery with general anesthesia
* Competent to provide informed consent

Exclusion Criteria:

* Emergency surgery
* Monitored Anesthesia Care (i.e., regional anesthesia alone without plans for general anesthesia)
* Surgery involving the eye, eyebrow, forehead, or frontal scalp near the sensor placement
* Poor health literacy
* Allergy, or have experienced any drug reaction to ketamine
* Pregnant or lactating
* Currently in active alcohol withdrawal
* Taking buprenorphine for chronic pain

Study Locations (1)

Emory University Hospital Midtown
Atlanta, Georgia, United States

This trial is not recruiting

This study is currently not accepting new participants.

Find recruiting trials
Data Source
ClinicalTrials.gov

Last updated from source