Status:
UNKNOWN
Incidence of Recall After Procedural Sedation With Propofol in the Emergency Department
Lead Sponsor:
Centre Hospitalier Universitaire de la Réunion
Conditions:
Fractures Reduction
Joint Dislocation Reduction
Eligibility:
All Genders
18+ years
Brief 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 .
Detailed 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 (...
Eligibility Criteria
Inclusion
- Adults patients (\> 18 years old) who had a procedural sedation in emergency department using propofol for fracture or joint dislocation reduction
- Patients who received an initial injection of Propofol by slow intravenous injection of 1 mg/kg in 20 seconds
- Inclusion less than 2 hours from the injection of Propofol
- Patients who have signed a consent to participate in the study
- Patients covered by social security.
Exclusion
- Patients under 18 years old
- Patients who cannot signed the informed consent
- Patients who had procedural sedation using other drugs that propofol
- Participation in another study type biomedical research
Key Trial Info
Start Date :
April 1 2014
Trial Type :
OBSERVATIONAL
Allocation :
ESTIMATED
End Date :
April 1 2017
Estimated Enrollment :
250 Patients enrolled
Trial Details
Trial ID
NCT02200744
Start Date
April 1 2014
End Date
April 1 2017
Last Update
February 4 2015
Active Locations (4)
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1
Groupe Hospitalier Est Réunion
Saint-Benoît, La Réunion, France, 97470
2
CHU de la Réunion
Saint-Denis, La Réunion, France, 97400
3
Centre Hospitalier Gabriel Martin
Saint-Paul, La Réunion, France, 97460
4
CHU de La Réunion
Saint-Pierre, La Réunion, France, 97448