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Incidence of Recall After Procedural Sedation With Propofol in the Emergency Department

NCT02200744 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 250

Last updated 2015-02-04

No results posted yet for this study

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 .

Conditions

  • Fractures Reduction
  • Joint Dislocation Reduction

Sponsors & Collaborators

  • Centre Hospitalier Universitaire de la Réunion

    lead OTHER

Principal Investigators

  • Pierre-Jean Marianne, MD · CHU de La Réunion

  • Marc Weber, MD · Groupe Hospitalier Est Réunion

  • Katia Mougin, MD · Centre Hospitalier Gabriel Martin

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2014-04-30
Primary Completion
2016-10-31
Completion
2017-04-30

Countries

  • France

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02200744 on ClinicalTrials.gov