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Clinical Trial Summary

The purpose of this study is to determine the incidence of recall in patients managed in emergency department with a procedural sedation protocol using propofol in a population of 250 .


Clinical Trial Description

After procedural sedation for fracture or joint dislocation reduction using propofol, adult patients recall will be assessed with a standardised form. This recall assessment will be realised 2 hours (+/- 15 minutes) after the procedural sedation and the day after.

The primary outcome measure will be the recall incidence 2 hours (+/- 15 minutes) after a procedural sedation. A secondary outcome will be the recall incidence one day after the procedural sedation.

The recall will be defined by a positive answer to the third question of the Sandin form (Lancet. 2000;355(9205):707-11). ;


Study Design

Observational Model: Cohort, Time Perspective: Prospective


Related Conditions & MeSH terms


NCT number NCT02200744
Study type Observational
Source Centre Hospitalier Universitaire de la Réunion
Contact Xavier Combes, MD
Phone 02 62 90 60 70
Email x.combes.samu974@chu-reunion.fr
Status Recruiting
Phase N/A
Start date April 2014
Completion date April 2017