Ireland
--:--IST
Recruiting Not applicable

Evaluation of Biomechanical Forced During the Practice of Endoscopic Retrograde Cholangiopancreatography

NCT07691580 · tracked via the Priya Life Science France tracker
Phase
Not applicable
Started
2026-06-08
Last updated
2026-07-10

Condition(s) studied

ERCPBiomechanicMusculoskeletal Disorders

Investigational drug(s) / intervention(s)

CAPTIV system

CAPTIV system: Each 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.

Study summary

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

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Adult subject (age ≥ 18 years) * hepato-gastroenterologist * Performing ERCP * Person who has given consent for participation in the study

Primary outcome measure(s)

  • measurement of average muscle during ERCP — 1 day
    measurement of average muscle during ERCP
  • measurement of angular analysis during ERCP — day 1

Trial sites (1)

FacilityCityRegionStatus
Centre Hospitalier Universitaire d'Amiens Amiens Picardie Recruiting

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07691580 on ClinicalTrials.gov ↗ ← All trials in France