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Enrolling by invitationOBSERVATIONAL

ESGE-Quality Improvement in Endoscopy: ERCP

This study, called 'ESGE-Quality Improvement in Endoscopy: ERCP', is investigating a tummy procedure called ERCP. The main goal is to see if new guidelines, put in place in 2017 by a group called the European Society of Gastrointestinal Endoscopy (ESGE), have helped to lower the chance of a problem called post-ERCP pancreatitis (PEP). Pancreatitis is a condition where the pancreas becomes inflamed. Researchers are comparing how often this problem happened before 2017, after 2017, and will continue to look at new cases from 2024 onwards. They hope that by improving the quality of ERCP procedures across Europe, fewer people will develop pancreatitis afterwards, making the procedure much safer for everyone.

At a glance

Status
Enrolling by invitation
Sponsor
Universität Münster
Enrolment target
1,254
Start
01 Jan 2024
Estimated completion
01 Jul 2026

What is this study about?

This study is all about improving the safety of a common medical procedure called ERCP. ERCP stands for Endoscopic Retrograde Cholangiopancreatography. It's a procedure where a doctor uses a thin, flexible tube with a camera to look at and treat problems in the tubes that connect your liver, gallbladder, and pancreas to your small intestine.

A known side effect of ERCP can be an inflamed pancreas, called pancreatitis. This study is looking at whether new guidelines, introduced in 2017 by a group named the European Society of Gastrointestinal Endoscopy (ESGE), have actually made ERCP procedures safer and reduced the number of people who get pancreatitis afterwards.

The researchers are comparing how often pancreatitis happened before these guidelines were introduced (before 2017), how often it's happened since (from 2017 to 2023), and they will continue to track this moving forward (from 2024). They hope to show that these quality improvements are making a real difference to patient safety and helping to ensure high standards of care across Europe.

Key takeaways

  • The study wants to make ERCP procedures safer.
  • It checks if new guidelines reduce a problem called pancreatitis after ERCP.
  • Information from your standard medical care is used, not extra tests.
  • You won't get new medicines or extra appointments because of the study.
  • The goal is to improve care for everyone having an ERCP in the future.

Who may be eligible?

To be part of this study, you need to be at least 18 years old and scheduled to have an ERCP procedure. The doctors want to make sure you understand what's involved and agree to take part.

However, there are some reasons why you might not be able to join. For example, if you are under 18, or if you are pregnant or breastfeeding, the study would not be suitable for you. Also, if you've already had more than one ERCP during your current hospital stay, only the first one would be considered.

Could this study suit you?

Answer these quick questions to see if you may be eligible. This is a guide only — the research team makes the final call.

  1. Are you 18 years old or older?
  2. Are you scheduled for an ERCP procedure?
  3. Are you able to understand information about the study?
  4. Are you NOT pregnant or breastfeeding?
  5. Have you had only one (or no) ERCPs during this hospital stay?
Answer every question to see your result.

What does participation involve?

This study is mainly looking at information that has already been collected or will be collected as part of your standard medical care during your ERCP procedure. You won't have to visit the clinic any extra times for this study, or have any additional tests or follow-up appointments. The researchers will be reviewing existing medical records and collecting information from ERCPs happening now and in the future. You won't be asked to take any new medications because of the study. The total duration of the study involves looking at information from before 2017, between 2017 and 2023, and then continuing to gather new information from 2024 onwards.

Potential risks and benefits

Taking part in this study primarily involves the researchers using information from your medical records related to your ERCP. For you, there are no direct personal benefits or extra risks beyond those already associated with having the ERCP procedure itself. The main benefit is that the study aims to improve the safety of ERCPs for future patients. You always have the right to withdraw your consent for your anonymised data to be used in the study at any time, without it affecting your medical care.

Locations (1)

  • University of Muenster, Josephs Hospital Warendorf, Academic Teaching Hospital
    Verified postcode
    Warendorf, Germany

Common questions

What is an ERCP procedure?

ERCP is a procedure using a thin tube with a camera to check and treat problems in the ducts of your liver, gallbladder, and pancreas.

What is post-ERCP pancreatitis (PEP)?

PEP is when your pancreas becomes inflamed after an ERCP procedure. It's a known, but uncommon, side effect.

Will taking part change my ERCP procedure?

No, taking part in this study will not change how your ERCP procedure is done or what care you receive.

Is my personal information kept private?

Yes, any information used from your medical records will be anonymised to protect your privacy.

Who is running this study?

This study is being run by researchers looking at guidelines from the European Society of Gastrointestinal Endoscopy (ESGE).

How to find out more

Always speak to your GP or specialist before deciding to take part in a study.

Interested in taking part?

Register your interest

Share your details and the research team for "ESGE-Quality Improvement in Endoscopy: ERCP…" will contact you if you may be eligible. Always speak to your GP before agreeing to take part.

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