Peptic Ulcer Perforation Study

NCT00624169 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 200

Last updated 2010-05-27

No results posted yet for this study

Summary

The objective of this study is to implement an optimized perioperative course for patients surgically treated for peptic ulcer perforation in order to improve the outcome for these patients.

The optimized perioperative course consists of a number of interventions carried out before, during and after surgery.

Conditions

  • Peptic Ulcer Perforation

Interventions

PROCEDURE

An optimized perioperative course

A number of interventions before, during and after surgery

Sponsors & Collaborators

  • Odense University Hospital

    collaborator OTHER
  • Bispebjerg Hospital

    collaborator OTHER
  • Hvidovre University Hospital

    collaborator OTHER
  • Aarhus University Hospital

    collaborator OTHER
  • Hillerod Hospital, Denmark

    collaborator OTHER
  • Helsingør hospital

    collaborator UNKNOWN
  • Copenhagen University Hospital at Herlev

    lead OTHER

Principal Investigators

  • Bo Belhage, MD, PhD · Department of Anaesthesiology and Intensive Care Medicine, Copenhagen University Hospital Bispebjerg

  • Lars N Jørgensen, MD, PhD · Department of Gastrointestinal Surgery, Copenhagen University Hospital Bispebjerg

  • Iben Rosenberg, MD · Department of Anaesthesiology and Intensive Care Medicine, Copenhagen University Hospital Hillerød

  • Anders U Neuenschwander, MD · Department of Gastrointestinal Surgery, Copenhagen University Hospital Hillerød

  • Ulf Sigild, MD · Department of Gastrointestinal Surgery, Copenhagen University Hospital Helsingør

  • Anne-Margrete Hedengran, MD · Department of Anaesthesiology and Intensive Care Medicine, Copenhagen University Hospital Helsingør

  • Peter Holde, MD · Department of Anaesthesiology and Intensive Care, Odense University Hospital

  • Erik Zimmermann-Nielsen, MD, PhD · Department of Gastrointestinal Surgery, Odense University Hospital

  • Anita Lauritsen, MD · Department of Anaesthesiology and Intensive Care Medicine, Århus University Hospital

  • Jørgen Bendix, MD · Department of Gastrointestinal Surgery, Århus University Hospital

  • Sven Adamsen, MD · Department of Gastrointestinal Surgery, Copenhagen University Hospital Herlev

  • Morten H Møller, MD · Department of Anaesthesiology and Intensive Care Medicine, Copenhagen University Hospital Herlev

  • Ann M Møller, MD, PhD · Department of Anaesthesiology and Intensive Care Medicine, Copenhagen University Hospital Herlev

  • Jens-Ulrik S Jensen, MD · Department of Clinical Microbiology / Copenhagen HIV Programme, Copenhagen University Hospital Hvidovre

  • Niels Fogh-Andersen, MD · Department of Clinical Biochemistry, Copenhagen University Hospital Herlev

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2007-11-30
Primary Completion
2009-12-31
Completion
2010-05-31

Countries

  • Denmark

Study Locations

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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 NCT00624169 on ClinicalTrials.gov