C67.8
Conditions
Interventions
Group 1: Prppective observational trial without intervention: informed consent prior to cystektomy with ileumconduit and health status as well as bacterial count in midstream urine, perioperative para
Sponsors
Universitätsmedizin Rostock,Urologische Klinik und Poliklinik
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: - age of 18, informed consent, ileum conduit after radical cystectomy
Exclusion criteria
Exclusion criteria: Not defined
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 1. Description of bacterial count in ileumconduit until 12 days ollowing surgery 2. Description of infection and retention paraclinics as well as performance status of these patients | — |
Secondary
| Measure | Time frame |
|---|---|
| 1. Risk stratefication of urinary tract infection following surgery, how much antibiotic therapy is really necessary | — |
Countries
Germany
Contacts
Public ContactLaila Schneidewind
Universitätsmedizin Rostock,Urologische Klinik und Poliklinik
Outcome results
None listed