CompletedPhase 1ketamine

Comparison of Two Intravenous Drug Combinations for Ambulatory Oral & Maxillofacial Surgery

Sponsored by Albert Einstein College of Medicine

NCT ID
NCT06867068
Target Enrollment
73 participants
Start Date
2016-10-04
Est. Completion
2024-06-10

About This Study

The purpose of this pilot study was to compare two commonly employed intravenous drug combinations; I) nitrous oxide, midazolam, fentanyl, and ketamine and II) the same combination with substitution of propofol for ketamine, for use during wisdom teeth extraction. Measures of recovery, amnesia testing 20 minutes after induction and after completion of recovery tests, patient satisfaction, and surgeon satisfaction will be evaluated. The data from this pilot study will be used to obtain preliminary estimates of effect sizes and to select primary and secondary endpoints for the design of a larger scale and more definitive trial of the two anesthetic approaches.

Conditions Studied

AnesthesiaTooth Extraction

Interventions

  • Midazolam Hydrochloride
  • Fentanyl
  • Ketamine
  • Propofol injection
  • Nitrous oxide

Eligibility

Age:16 Years - N/A
Healthy Volunteers:Yes
View full eligibility criteria
Inclusion Criteria:

* American Society of Anesthesiologists (ASA) health class I or II
* Existing clinical population

Exclusion Criteria:

* Do not meet the Inclusion Criteria

Study Locations (1)

NYCHHC - Jacobi Medical Center and North Central Bronx Hospital
The Bronx, New York, 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