Clinical Trials Directory

Trials / Completed

CompletedNCT00997321

Propofol Versus Ketamine for Moderate Procedural Sedation in the Emergency Department (ED)

Propofol Versus Ketamine for Procedural Sedation During Painful Procedures in the Emergency Department

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
100 (actual)
Sponsor
Hennepin Healthcare Research Institute · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

This study is a clinical trial of moderate sedation with propofol versus moderate sedation with ketamine for procedural sedation in the Emergency Department.

Conditions

Interventions

TypeNameDescription
DRUGpropofolpropofol 1 millgram per kilogram intravenous bolus followed by 0.5 milligrams per kilogram as needed for moderate procedural sedation
DRUGKetamineketamine milligram per kilogram followed by 0.5 milligrams per kilogram as need for moderate procedural sedation

Timeline

Start date
2007-07-01
Primary completion
2009-10-01
Completion
2009-10-01
First posted
2009-10-19
Last updated
2012-04-02
Results posted
2012-03-26

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT00997321. Inclusion in this directory is not an endorsement.

Propofol Versus Ketamine for Moderate Procedural Sedation in the Emergency Department (ED) (NCT00997321) · Clinical Trials Directory