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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03232840
Other study ID # RECHMPL17_0228
Secondary ID
Status Completed
Phase
First received
Last updated
Start date July 31, 2017
Est. completion date December 31, 2018

Study information

Verified date October 2018
Source University Hospital, Montpellier
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial 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 wrong site surgery during anesthesia.


Description:

Before the study, the investigators selected 7 preventive measures to avoid wrong site surgery during regional anesthesia combined or not with general anesthesia . These measures were learned to the entire anesthesia team (nurse, resident and anesthesiologist) during conventional meetings. An initial evaluation of the application of these measures will be carried out before the introduction of e-learning. This assessment will be conducted by nurses without the knowledge of the anesthetic team evaluated. After this initial evaluation, e-learning will be broadcast on the hospital intranet. Then a second evaluation of the application of the preventive measures will be carried out 6 month and 1 year after the introduction of e-learning.


Recruitment information / eligibility

Status Completed
Enrollment 100
Est. completion date December 31, 2018
Est. primary completion date October 30, 2018
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion criteria:

- patient undergoing regional anesthesia with or without general anesthesia

Exclusion criteria:

- general anesthesia without regional anesthesia

- perimedullar anesthesia

- bilateral surgery

Study Design


Related Conditions & MeSH terms

  • Medical Errors : Wrong Site Surgery in Regional Anesthesia

Locations

Country Name City State
France Uhmontpellier Montpellier

Sponsors (1)

Lead Sponsor Collaborator
University Hospital, Montpellier

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Other Assessment of the application of each of the 7 preventive measures according to various clinical parameters Evaluation of the application of each of the 7 preventive measures according to the clinical parameters of the patients followed (age of the patient, ASA physical status, type of surgery, type of anesthesia, period of the day or week, Emergency or elective). 1 day
Other Evaluation of the application of the preventive measures following the introduction of the e-learning in the anesthesia team. Evaluation of the application of the preventive measures following the introduction of the e-learning in the anesthesia team. 6 month and 1 year
Primary Evaluation of the application of each of the 7 preventive measures using a questionnaire filled by a nurse not involved in the regional anesthesia procedure Evaluation of the application of each of the 7 preventive measures using a questionnaire filled by a nurse not involved in the regional anesthesia procedure. This questionnaire simply indicates whether a measure has been applied or not 1 day