FindTrial
Sign In

Peptic Ulcer Perforation Study

Peptic Ulcer Perforation Study - an Optimized Perioperative Course for Patients Surgically Treated for Peptic Ulcer Perforation

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00624169
Acronym
PULP
Enrollment
200
Registered
2008-02-26
Start date
2007-11-30
Completion date
2010-05-31
Last updated
2010-05-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Peptic Ulcer Perforation

Keywords

Perforated peptic ulcer, Mortality

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.

Interventions

PROCEDUREAn optimized perioperative course

A number of interventions before, during and after surgery

Sponsors

Odense University Hospital
CollaboratorOTHER
Bispebjerg Hospital
CollaboratorOTHER
Hvidovre University Hospital
CollaboratorOTHER
Aarhus University Hospital
CollaboratorOTHER
Hillerod Hospital, Denmark
CollaboratorOTHER
Helsingør hospital
CollaboratorUNKNOWN
Copenhagen University Hospital at Herlev
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Patients surgically treated for benign peptic ulcer perforation

Exclusion criteria

* Age \< 18 years * Pregnant and breastfeeding women * Malign ulcer perforation

Design outcomes

Primary

MeasureTime frame
All cause mortality rateWithin 30 days of surgery

Countries

Denmark

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 29, 2026