K56.0
Conditions
Interventions
Group 1: In this study, patients with Ogilvie's syndrome are retrospectively evaluated regarding the treatment they received (conservative, endoscopic, surgical) and the therapeutic succes. In this co
Sponsors
Universitätsklinikum Freiburg, Departemnt Chirurgie, Klinik für Allgemein- und Viszeralchirurgie
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: all patients who were treated for Ogilvie's Syndrome between 2002 and 2019 at the University Medical Center Freiburg, Germany, Department for General and Viszeral Surgery
Exclusion criteria
Exclusion criteria: age less than 18 years
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Primary endpoint of this study is therapeutic success which is examined in a time frame of 7 days after initiation of treatment by clinical presentation of the patients, bowel movement and lab results (CRP, leukocytes, lactat). | — |
Secondary
| Measure | Time frame |
|---|---|
| morbidity, longterm outcome | — |
Countries
Germany
Contacts
Public ContactLampros Kousoulas
Universitätsklinikum Freiburg, Departemnt Chirurgie, Klinik für Allgemein- und Viszeralchirurgie
Outcome results
None listed