Clinical Trials Logo

Clinical Trial 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.


Clinical Trial Description

n/a


Study Design

Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


NCT number NCT00624169
Study type Interventional
Source Copenhagen University Hospital at Herlev
Contact
Status Completed
Phase N/A
Start date November 2007
Completion date May 2010

See also
  Status Clinical Trial Phase
Completed NCT01620671 - Fast-track Surgery for Perforated Peptic Ulcers Phase 4
Completed NCT01376414 - H. Pylori Testing for Patients With Non-specific Upper Abdominal Pain in the Emergency Department N/A
Recruiting NCT06042933 - Early Oral Feeding Versus Traditional Delayed Oral Feeding Post-perforated Peptic Ulcer Repair N/A
Completed NCT04194060 - ERAS vs Conventional Approach in Peptic Perforation-RCT N/A
Recruiting NCT04447170 - Laparoscopic Versus Open Repair of Peptic Ulcer Perforation
Completed NCT05489497 - Morbidity After Surgical Treatment of Perforated Ulcer