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Closed-loop Sedation of Propofol for Patients Undergoing Spinal Anesthesia

NCT01020643 · Status: COMPLETED · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 203

Last updated 2013-10-25

No results posted yet for this study

Summary

The purpose of this study is to compare the administration of a standard anesthetic drug (propofol) using an automatic, expert-based system versus a manually controlled system by the anesthesiologist. In addition, the performance of the decision support system will be evaluated.

Conditions

  • Conscious Sedation

Interventions

DRUG

controlled administration of propofol

comparison of propofol sedation

Sponsors & Collaborators

  • Thomas Hemmerling

    lead OTHER

Principal Investigators

  • Thomas Hemmerling, MD · MUHC - MGH

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

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

Timeline & Regulatory

Start
2009-11-30
Primary Completion
2011-08-31
Completion
2011-08-31

Countries

  • Canada

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 NCT01020643 on ClinicalTrials.gov