PROTon Pump Inhibitors and Stent OCclusion Rate Of Lumen Apposing Metal Stents

NCT05817721 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 893

Last updated 2025-06-15

No results posted yet for this study

Summary

The goal of this observational retrospective cohort study in combination with an expert study is to assess the clinical relevance and management of Lumen apposing metal stent (LAMS)-occlusion and LAMS-occlusion-related complications as well as the influence of proton pump inhibitors (PPI) on LAMS-occlusion.

The main questions this study aims to answer are:

* the individual management of LAMS-occlusion and LAMS-occlusion-related complications in the respective centers participating in the study.
* if there is an association between PPI-intake and LAMS-occlusion and endoscopic necrosectomies.

Participants for the retrospective cohort study will be enrolled retrospectively among European centers with expertise in pancreatology. The expert survey will be distributed European-wide to centers with special expertise in pancreatology.

Conditions

Interventions

DRUG

Proton pump inhibitor

Patients who received a lumen apposing metal stent (LAMS) for drainage of a walled off necrosis (WON) upon acute pancreatitis will be divided into a PPI/Non-PPI group depending on if they concomitantly were prescribed a PPI or not

DEVICE

LAMS-implantation

Patients who received a lumen apposing metal stent (LAMS) for drainage of a walled off necrosis (WON) upon acute pancreatitis

Sponsors & Collaborators

  • Technical University of Munich

    collaborator OTHER
  • Ludwig-Maximilians - University of Munich

    collaborator OTHER
  • University Hospital in Halle

    collaborator OTHER
  • University of Leipzig

    collaborator OTHER
  • University Hospital Heidelberg

    collaborator OTHER
  • Landesklinikum Sankt Polten

    collaborator OTHER
  • University Hospital, Aachen

    collaborator OTHER
  • University of Oldenburg

    collaborator OTHER
  • University of Newcastle Upon-Tyne

    collaborator OTHER
  • Szeged University

    collaborator OTHER
  • University of Pecs

    collaborator OTHER
  • Semmelweis University

    collaborator OTHER
  • University of Ulm

    collaborator OTHER
  • University Hospital Olomouc

    collaborator OTHER
  • Brno University Hospital

    collaborator OTHER
  • University Hospital Regensburg

    collaborator OTHER
  • Klinikum Stadt Hanau

    collaborator OTHER
  • University Medicine Greifswald

    collaborator OTHER
  • University Medical Center Goettingen

    lead OTHER

Principal Investigators

  • Jacob Hamm · Department of Gastroenterology, University Hopsital Goettingen

  • Christoph Ammer-Herrmenau, MD · Department of Gastroenterology, University Hopsital Goettingen

  • Volker Ellenrieder, Professor · Department of Gastroenterology, University Hopsital Goettingen

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2023-05-05
Primary Completion
2024-03-29
Completion
2024-03-29

Countries

  • Germany

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05817721 on ClinicalTrials.gov