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Race-Specific Propofol Titration to Effect for Procedural Sedation

NCT03290859 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 2780

Last updated 2019-10-25

No results posted yet for this study

Summary

Prospectively evaluate newly established guidelines and make clinicians aware of inter-racial difference in propofol sensitivity.

Conditions

  • Unconsciousness
  • Apnea, Postanesthetic
  • Sedative Overdose
  • Hypoxemia

Interventions

PROCEDURE

Titrate propofol monotherapy infusion to effect

Train anesthesia providers in a standardized protocol for titrating propofol infusion to effect.

Sponsors & Collaborators

  • National Center for Advancing Translational Sciences (NCATS)

    collaborator NIH

  • University of Florida

    lead OTHER

Principal Investigators

  • Jeffrey White, MD · University of Florida

Eligibility

Min Age
18 Years
Max Age
80 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2018-01-05
Primary Completion
2019-02-05
Completion
2019-02-05

Countries

  • United States

Study Locations

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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 NCT03290859 on ClinicalTrials.gov