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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT06164171
Other study ID # 7646
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date June 9, 2020
Est. completion date December 31, 2023

Study information

Verified date December 2023
Source University Hospital, Strasbourg, France
Contact Walid OULEHRI, MD
Phone 33 3 69 55 12 71
Email walid.oulehri@chru-strasbourg.fr
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Transesophageal echocardiography (TEE) has gradually become the technique of choice for continuous functional examination of the heart despite the significant training required for its interpretation. It has proven to be the safest, fastest, and most reliable technique for diagnosing most intra- and postoperative hemodynamic problems. Indeed, the transesophageal route is particularly well adapted to the situation of intubated patients, whether in the operating room, in the outpatient department or in intensive care. It offers images that are easier to obtain and of better quality than the transthoracic route; it can be performed without interfering with surgical activity or resuscitation. However, TEE training is often poor during the DES training in anesthesia and resuscitation, reserved for the few interns who will learn in a specific department where TEE is used on a daily basis. Thus, simulation is a logical and recognized means by which technical aspects, mechanisms involved in the understanding of a situation, reasoning and decision making can be analyzed and improved. The RFE SFAR 2019 recommendations suggest the use of simulation for the learning of technical gestures in initial training in order to improve their acquisition. This study is therefore part of a technical and diagnostic improvement of a practice, which appears to be essential in several fields in anesthesia and intensive care, for a technique still not sufficiently acquired by many future practitioners.


Recruitment information / eligibility

Status Recruiting
Enrollment 26
Est. completion date December 31, 2023
Est. primary completion date December 2023
Accepts healthy volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion criteria: - 1st or 2nd year DESAR interns who participated in the continuing education program - Interns who agreed to participate in the professional practice evaluation study Exclusion criteria : - Interns who did not participate in the training - Residents who do not agree to take the final test

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
France Service de Réanimation Chirurgicale - CHU de Strasbourg - France Strasbourg

Sponsors (1)

Lead Sponsor Collaborator
University Hospital, Strasbourg, France

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Ability of a population of medical students to perform a TEE thanks to the contribution of simulation to their learning compared to a population of interns not trained on a high definition simulator Time in seconds required to make the 11 cuts 1 hour after operation
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