Influence of Resident's Degree of Formation on the Quality of Care Delivered to the Patients.

January 9, 2019 updated by: Eric DEFLANDRE, MD, PhD, FCCP, FAHA, Astes
The aim of this study is to evaluation the influence of the resident in anesthesiology's degree of formation on the quality of care delivered to the patient.

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Detailed Description

The aim of this study is to evaluation the influence of the resident in anesthesiology's degree of formation on the quality of care delivered to the patient.

To perform it, the investigators will enrolled all of the patients scheduled for an axillary plexus anesthesia technique in the Clinique Saint-Luc of Bouge in September 2018 (end of formation for the residents in anesthesia) and compare the patient's degree of satisfaction with the patients scheduled for the same kind of anesthesia on October and November 2018 (begin of formation for the residents in anesthesia).

Study Type

Observational

Enrollment (Actual)

188

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

  • Belgium
      • Namur, Belgium, 5004
        • Clinique Saint-Luc Bouge

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

N/A

Genders Eligible for Study

All

Sampling Method

Probability Sample

Study Population

All patients scheduled for hand surgery under axillary plexus in the Clinique Saint-Luc of Bouge (Namur, Belgium)

Description

Inclusion Criteria:

  • All patients scheduled for hand surgery under axillary plexus

Exclusion Criteria:

  • Patient's refusal

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
End of training
Anesthesia residents at the end of their training who will realize axillary plexus. The satisfaction of the patient will be registered.
Biological: Axillary Plexus
Axillary plexus anesthesia technique for hand surgery
Begin of training
Anesthesia residents at the begin of their training who will realize axillary plexus. The satisfaction of the patient will be registered.
Biological: Axillary Plexus
Axillary plexus anesthesia technique for hand surgery

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Patient satisfaction (Likert's scale)
Time Frame: 1 day
Patient satisfaction after the completion of axillary plexus (satisfaction will be studied with a Lickert's scale). This scale will examine the patient's satisfaction in a scale ranging from 0 (worse satisfaction) to 5 (best satisfaction).
1 day

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Astes

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

September 1, 2018

Primary Completion (Actual)

November 16, 2018

Study Completion (Actual)

January 1, 2019

Study Registration Dates

First Submitted

November 14, 2018

First Submitted That Met QC Criteria

November 15, 2018

First Posted (Actual)

November 16, 2018

Study Record Updates

Last Update Posted (Actual)

January 10, 2019

Last Update Submitted That Met QC Criteria

January 9, 2019

Last Verified

January 1, 2019

More Information

Terms related to this study

Other Study ID Numbers

  • PQR

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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