About this trial
A number of best practice recommendations have been developed to improve practitioner comfort, similar to those recommended for digestive surgeons. It is recommended to use a height-adjustable examination table, position the screen at eye level, and use a chair during the procedure. The use of lead aprons is essential for certain endoscopic procedures (ERCP drainage of the bile ducts, prosthesis placement, etc.). Several retrospective studies in the surgical and radiological fields have shown an increased risk of MSDs among these populations. To distribute the weight of the apron, several shapes are available to limit stress. An apron weighs approximately 7 kg, due in particular to the amount of lead. The aim of this study is to evaluate the biomechanical forced experienced by the gastroenterologist during ERCP.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Adult subject (age ≥ 18 years)
hepato-gastroenterologist
Performing ERCP
Person who has given consent for participation in the study
Disqualifiers
None
Trial design
Single group
Treatments tested in this trial
CAPTIV system
DeviceEach practitioner will perform 4 ERCP recorded using the CAPTIV system. In order to know the biomechanical constraints during standard endoscopic examination (upper endoscopy and colonoscopy), an upper endoscopy and a standard colonoscopy examination will also be filmed and monitored.
Treatment groups
Trial outcomes
Primary outcomes
measurement of average muscle during ERCP
measurement of average muscle during ERCP
measurement of angular analysis during ERCP
Secondary outcomes
level of stress during the practice of ERCP
level of stress during the practice of ERCP by analyzing the average data obtained from cardiofrequency monitoring
Sponsors and contacts
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Centre Hospitalier Universitaire, Amiens
Lead sponsor
Central Hospital, Nancy, France
Collaborator
University Hospital, Caen
Collaborator
Clinique de l'Europe, Amiens
Collaborator
Hôpital Privé Saint-Claude, Saint Quentin
Collaborator