MedTrace Logo

Propofol Sedation Study

NCT00597740 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 57

Last updated 2013-12-03

No results posted yet for this study

Summary

Purpose of Protocol: The purpose of this study will be to compare the clinical utility of Propofol sedation with and without the use of the ICU Sedation Protocol. Patients will be treated according to the attending/consulting preference. No attempt will be made to influence the patient's routine care and management. The study will compare the average hourly infusion rates for the Propofol administration, as well as obtain the nursing staffs evaluation regarding the ease of neurological assessment during each 12 hour shift

Conditions

  • Anesthesia

Sponsors & Collaborators

  • Scottsdale Healthcare

    lead OTHER

Principal Investigators

  • Joseph Zabramski, MD · Scottsdale Healthcare Osborn - Neurosurgery

Eligibility

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

Timeline & Regulatory

Start
2007-12-31
Primary Completion
2010-09-30
Completion
2013-12-31

Countries

  • United States

Study Locations

More Related Trials

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 NCT00597740 on ClinicalTrials.gov