Evaluation of Biomechanical Forced During the Practice of Endoscopic Retrograde Cholangiopancreatography

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorCentre Hospitalier Universitaire, Amiens

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 volunteers

Qualifiers

Adult subject (age ≥ 18 years)

hepato-gastroenterologist

Performing ERCP

Person who has given consent for participation in the study

Disqualifiers

None

Trial design

Design model

Single group

Treatments tested in this trial

  • CAPTIV system

    Device

    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.

Treatment groups

10 Participants
are divided into 1 treatment group
Group A: CAPTIV systemExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

measurement of average muscle during ERCP

measurement of average muscle during ERCP

Time frame
1 day
2

measurement of angular analysis during ERCP

Time frame
day 1

Secondary outcomes

1

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

Time frame
day 1

Other outcomes

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