Predictive Factors for 10-year Biochemical Recurrence and Urinary Continence Following Robot-assisted Radical Prostatectomy for Prostate Cancer
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: Radical prostatectomy.
- Who it may be relevant to
- Registry conditions: Prostate Cancer (Adenocarcinoma). Basic parameters: No limits · Male.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- Slovakia
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
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Official title
Ten-Year Oncologic and Functional Results of Prostate Cancer Treatment by Radical Prostatectomy and the Rate of Patient Satisfaction
Overview
The aim of the present project is to evaluate long-term oncological and functional treatment outcomes, as well as patient satisfaction, ten years after radical prostatectomy in patients initially enrolled in CPRRP study. This research builds on a previous five-year follow-up evaluation (approved by the ethics committee) and focuses on the durability of therapeutic effects, quality of life, and long-term complications. Data will be collected via telephone interviews assessing key parameters (PSA levels, information on subsequent radiotherapy and androgen-deprivation therapy, the ICIQ-SF and IIEF-5 questionnaires, and patient-reported quality-of-life and satisfaction measures), followed by statistical analysis.
Interventions
- Procedure Radical prostatectomy
Robot assisted radical prostatectomy
Primary outcome measures
- Biochemical recurrence [Time frame: From treatment to 10 years.]
Secondary outcome measures (2)
- Incontinence rate [Time frame: From surgery until 10 years.]
- Erectile dysfunction rate [Time frame: From surgery until 10 years.]
Eligibility criteria
Inclusion criteria
- Robot assisted radical prostatectomy performed in CPRRP study
Exclusion criteria
\-
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Observational model
- Cohort
Study locations
Slovakia · 1 center
- F.D. Roosvelt university hospital — Banská Bystrica
Identifiers
NCT: NCT07439913 · CPRRP10