Peptic Ulcer Perforation Clinical Trial
— PULPOfficial title:
Peptic Ulcer Perforation Study - an Optimized Perioperative Course for Patients Surgically Treated for Peptic Ulcer Perforation
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.
Status | Completed |
Enrollment | 200 |
Est. completion date | May 2010 |
Est. primary completion date | December 2009 |
Accepts healthy volunteers | No |
Gender | Both |
Age group | 18 Years and older |
Eligibility |
Inclusion Criteria: - Patients surgically treated for benign peptic ulcer perforation Exclusion Criteria: - Age < 18 years - Pregnant and breastfeeding women - Malign ulcer perforation |
Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment
Country | Name | City | State |
---|---|---|---|
Denmark | Århus University Hospital | Århus | |
Denmark | Copenhagen University Hospital Bispebjerg | Copenhagen NV | |
Denmark | Copenhagen University Hospital Helsingør | Helsingor | |
Denmark | Copenhagen University Hospital Herlev | Herlev | |
Denmark | Copenhagen University Hospital Hillerød | Hillerød | |
Denmark | Copenhagen University Hospital Hvidovre | Hvidovre | |
Denmark | Odense University Hospital | Odense |
Lead Sponsor | Collaborator |
---|---|
Copenhagen University Hospital at Herlev | Aarhus University Hospital, Bispebjerg Hospital, Helsingør hospital, Hillerod Hospital, Denmark, Hvidovre University Hospital, Odense University Hospital |
Denmark,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | All cause mortality rate | Within 30 days of surgery | No |
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