NCT00715507

Brief Summary

To assess the clinical utility of the graphical medication monitor, results of the anesthetics for which the display was present will be compared to the results of the anesthetics in which there was no display.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
200

participants targeted

Target at P75+ for all trials

Timeline
Completed

Started Jul 2003

Longer than P75 for all trials

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

July 1, 2003

Completed
5 years until next milestone

First Submitted

Initial submission to the registry

July 11, 2008

Completed
4 days until next milestone

First Posted

Study publicly available on registry

July 15, 2008

Completed
4 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

August 1, 2012

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

August 1, 2012

Completed
Last Updated

August 10, 2016

Status Verified

August 1, 2016

Enrollment Period

9.1 years

First QC Date

July 11, 2008

Last Update Submit

August 8, 2016

Conditions

Decision Making

Keywords

decision makinggraphic display

Outcome Measures

Primary Outcomes (1)

  • assess differences between medication administration data and patient information with and without the use of the graphical medication monitor.

    preoperative, intraoperative and postoperative

Study Arms (2)

1

For the phase of the study in which the utility of the graphical medication monitor is assessed, the monitor will not be shown to anesthesiologists placed in the control condition.

2

In the experimental condition, anesthesiologists will be shown the medication monitor to aid their expertise and decision-making.

Device: medication monitor

Interventions

medication monitorDEVICE

the medication monitor will aid in expertise and decision-making.

2

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

Board certified attending anesthesiologists at the University of Utah Health Sciences Center and supervised anesthesiology residents

You may qualify if:

  • Board certified attending anesthesiologists at the University of Utah Health Sciences Center and supervised anesthesiology residents and have been trained on the graphic display

You may not qualify if:

  • Board certified attending anesthesiologists at the University of Utah Health Sciences Center and supervised anesthesiology residents that have not been trained on the graphic display

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

University of Utah

Salt Lake City, Utah, 84132, United States

Location

Study Officials

  • Ken Johnson

    University of Utah

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
observational
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
MS

Study Record Dates

First Submitted

July 11, 2008

First Posted

July 15, 2008

Study Start

July 1, 2003

Primary Completion

August 1, 2012

Study Completion

August 1, 2012

Last Updated

August 10, 2016

Record last verified: 2016-08

Locations

US(1)