NCT03232853

Brief Summary

The purpose of this observational study is to assess the efficiency of an e-learning in order to put into practice some preventive measures to avoid medication errors during anesthesia.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
100

participants targeted

Target at P50-P75 for all trials

Timeline
Completed

Started Jul 2017

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

July 5, 2017

Completed
23 days until next milestone

First Posted

Study publicly available on registry

July 28, 2017

Completed
3 days until next milestone

Study Start

First participant enrolled

July 31, 2017

Completed
1.3 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

November 30, 2018

Completed
1 month until next milestone

Study Completion

Last participant's last visit for all outcomes

December 31, 2018

Completed
Last Updated

April 18, 2019

Status Verified

September 1, 2018

Enrollment Period

1.3 years

First QC Date

July 5, 2017

Last Update Submit

April 17, 2019

Conditions

Keywords

medical error in anesthesiadrug error in anesthesia

Outcome Measures

Primary Outcomes (1)

  • Percentage of application of the preventive measures after versus before the use of an e-learning.

    Percentage of application of the preventive measures after versus before the use of an e-learning.

    1 day

Secondary Outcomes (1)

  • Evaluation of the application of each of the 15 preventive measureaccording to various clinical parameters

    1 day

Other Outcomes (1)

  • Evaluation of the application of the preventive measures following the introduction of the e-learning in the anesthesia team.

    6 month and 1 year

Interventions

Elearning

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

Patients undergoing anesthesia in Lapeyronie Hospital

You may qualify if:

  • patient undergoing regional and/or general anesthesia

You may not qualify if:

  • only sedation

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Uhmontpellier

Montpellier, 34295, France

Location

Study Officials

  • BIBOULET Philippe, MD, PhD

    University Hospital, Montpellier

    STUDY DIRECTOR

Study Design

Study Type
observational
Observational Model
OTHER
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

July 5, 2017

First Posted

July 28, 2017

Study Start

July 31, 2017

Primary Completion

November 30, 2018

Study Completion

December 31, 2018

Last Updated

April 18, 2019

Record last verified: 2018-09

Locations