Try the modernized ClinicalTrials.gov beta website. Learn more about the modernization effort.
Working…
ClinicalTrials.gov
ClinicalTrials.gov Menu

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

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
 
ClinicalTrials.gov Identifier: NCT03744455
Recruitment Status : Completed
First Posted : November 16, 2018
Last Update Posted : January 10, 2019
Sponsor:
Information provided by (Responsible Party):
Eric DEFLANDRE, MD, PhD, FCCP, FAHA, Astes

Brief Summary:
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.

Condition or disease Intervention/treatment
Anesthesia Complication Biological: Axillary Plexus

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).

Layout table for study information
Study Type : Observational
Actual Enrollment : 188 participants
Observational Model: Cohort
Time Perspective: Prospective
Official Title: Influence of Resident's Degree of Formation on the Quality of Care Delivered to the Patients.
Actual Study Start Date : September 1, 2018
Actual Primary Completion Date : November 16, 2018
Actual Study Completion Date : January 1, 2019

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




Primary Outcome Measures :
  1. 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).



Information from the National Library of Medicine

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.


Layout table for eligibility information
Ages Eligible for Study:   18 Years and older   (Adult, Older Adult)
Sexes 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)
Criteria

Inclusion Criteria:

  • All patients scheduled for hand surgery under axillary plexus

Exclusion Criteria:

  • Patient's refusal

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03744455


Locations
Layout table for location information
Belgium
Clinique Saint-Luc Bouge
Namur, Belgium, 5004
Sponsors and Collaborators
Astes
Investigators
Layout table for investigator information
Principal Investigator: Eric Deflandre, MD, PhD Astes
Layout table for additonal information
Responsible Party: Eric DEFLANDRE, MD, PhD, FCCP, FAHA, Head of Department, Astes
ClinicalTrials.gov Identifier: NCT03744455    
Other Study ID Numbers: PQR
First Posted: November 16, 2018    Key Record Dates
Last Update Posted: January 10, 2019
Last Verified: January 2019

Layout table for additional information
Studies a U.S. FDA-regulated Drug Product: No
Studies a U.S. FDA-regulated Device Product: No