Peptic Ulcer Perforation Study

Not Applicable

Completed

• Conditions: Peptic Ulcer Perforation

• Registration Number: NCT00624169
• Lead Sponsor: Copenhagen University Hospital at Herlev

Brief 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.

Detailed Description

Not available

Study Timeline

• Study Start: 2007-11
• Study First Submitted: 2008-02-15
• Study First Submitted QC: 2008-02-15
• Study First Posted: 2008-02-26
• Primary Completion: 2009-12
• Status Verified: 2010-05
• Study Completion: 2010-05
• Last Update Submitted: 2010-05-26
• Last Update Posted: 2010-05-27

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 200

Inclusion Criteria

• Patients surgically treated for benign peptic ulcer perforation

Exclusion Criteria

• Age < 18 years
• Pregnant and breastfeeding women
• Malign ulcer perforation

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: SINGLE_GROUP

Primary Outcome Measures

Name	Time	Method
All cause mortality rate	Within 30 days of surgery

Trial Locations

Locations (7)

Copenhagen University Hospital Hillerød; 🇩🇰 Hillerød, Denmark

Copenhagen University Hospital Herlev; 🇩🇰 Herlev, Denmark

Copenhagen University Hospital Bispebjerg; 🇩🇰 Copenhagen NV, Denmark

Copenhagen University Hospital Helsingør; 🇩🇰 Helsingor, Denmark

Århus University Hospital; 🇩🇰 Århus, Denmark

Copenhagen University Hospital Hvidovre; 🇩🇰 Hvidovre, Denmark

Odense University Hospital; 🇩🇰 Odense, Denmark