CompletedPhase 4ketamine

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

NCT ID

NCT00997321

Target Enrollment

100 participants

Start Date

2007-07

Est. Completion

2009-10

About This Study

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

Conditions Studied

Sedation

Interventions

•propofol
•Ketamine

Eligibility

Age:18 Years - N/A

Healthy Volunteers:No

View full eligibility criteria

Inclusion Criteria:

* patients who require moderate procedural sedation with propofol in the ED

Exclusion Criteria:

* age \> 17 years
* pregnant
* intoxicated
* cannot give informed consent
* allergy to ketamine or propofol
* patient will require deep procedural sedation
* ASA physical status score \> 2

Study Locations (1)

Hennepin County Medical Center

Minneapolis, Minnesota, United States