CompletedN/Aketamine

Evaluation of Closed-loop TIVA Propofol, Sufentanil and Ketamine Guided by BIS Monitor

Sponsored by The University of Texas Health Science Center at San Antonio

NCT ID
NCT01942356
Target Enrollment
4 participants
Start Date
2013-09
Est. Completion
2014-08

About This Study

The purpose of this study is to compare a closed-loop intravenous anesthetic using Bispectral Index as a feedback loop and a controller based on reinforcement learning to titrate dose and intravenous anesthetic that is manually controlled or a standard volatile anesthetic agent titrated by the anesthesiologist to determine improvement in the following parameters as compared to controls: time to discharge from the Post Anesthesia Care Unit, post-operative nausea and vomiting, pain scores and sedation scores.

Conditions Studied

Acute CholecystitisChronic Cholecystitis

Interventions

  • TIVA - Hypotension
  • TIVA - Hypertension
  • TIVA - Bradycardia
  • TIVA - Tachycardia
  • INH - Hypotension
  • INH - Hypertension
  • INH - Bradycardia
  • INH - Tachycardia

Eligibility

Age:18 Years - 65 Years
Healthy Volunteers:Yes
View full eligibility criteria
Inclusion Criteria:

* 18-65 years of age
* Body mass index lower or equal to 40 m2/kg
* Subjects must be able to comprehend spoken and written English or Spanish

Exclusion Criteria:

* Any type of psychiatric, neurological, or neuromuscular disorder
* Thyroid disease
* Alcohol consumption which exceeds 2 drinks per day and/or drug abuse.
* Allergy to study medication proposal, soy or egg proteins
* history of drug abuse
* chronic or acute use of opioids, or other medications affecting the central nervous system
* pregnancy

Study Locations (1)

University Hospital
San Antonio, Texas, 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