C61
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1) Patients must have taken part in the HAROW study and have consented to long-term follow-up. 2) Patients must have undergone either retropubic or robotic-assisted radical prostatectomy. 3) Patient data must have been sufficient for analysis in the HAROW study. Inclusion criteria from the HAROW study: 4) Newly diagnosed patients with a prostate cancer that is limited to the prostate gland (max. tumor staging T2c) 5) Patients without known metastases (N0, M0)
Exclusion criteria
Exclusion criteria: 1) Recurrence of prostate cancer 2) Tumor staging T3 or greater
Design outcomes
Secondary
| Measure | Time frame |
|---|---|
| Secondary endpoints are decisional regret (Decision regret scale), the retrospective judgment of the decision-making process (Degner scale) and quality of life (EORTC-QOL-30). | — |
Primary
| Measure | Time frame |
|---|---|
| Primary endpoint is to compare long-term functional outcome (EPIC-26). | — |
Countries
Germany
Contacts
SMG Forschungsgesellschaft mbH