C64 C67
Conditions
Interventions
Group 1: Standard of care, high-risk patient (EI=4), no intervention
Estimation of ADL and colecting blood samples (biomarker) prior to operation, at discharge, after 1,3 and 6 months postoperatively.
Sponsors
Urologische und Kinderurologische Klinik, Uniklinikum Erlangen
Eligibility
Sex/Gender
All
Age
65 Years to No maximum
Inclusion criteria
Inclusion criteria: Planned radical Cystektomy or Kidney operation in curative intention
Exclusion criteria
Exclusion criteria: Age under 65 years, metastatic disease, neoadjuvant chemotherapy
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Functional deterioration, defined as ADL-reduction. Endpoint ist estimated 1, 3 and 6 months after operation. | — |
Secondary
| Measure | Time frame |
|---|---|
| Overall mortality | — |
Countries
Germany
Contacts
Public ContactChristian Fiebig
Urologische und Kinderurologische Klinik, Uniklinikum Erlangen
Outcome results
None listed