Prospective clinical study on quality of life and sexuality after robotic radical cystectomy

Prospective clinical study on quality of life and sexuality after robotic radical cystectomy - ROSY-Q

Status

Recruiting

Phases

Unknown

Study type

Observational

Source

DRKS

Registry ID

DRKS00035746

Enrollment

140

Registered

2025-02-04

Start date

2025-01-31

Completion date

Unknown

Last updated

2025-04-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

C67.9

Interventions

Group 1: The patient group includes all adult patients capable of giving consent who undergo robotic radical cystectomy with an oncological indication at the uro-oncology centre of the UKSH Campus Kie

Eligibility

Sex/Gender

All

Age

18 Years to No maximum

Inclusion criteria

Inclusion criteria: Oncological indication for radical cystectomy

Exclusion criteria

Exclusion criteria: Persons not capable of giving consent Particularly vulnerable groups (e.g. persons with disabilities) Conversion to open radical cystectomy

Design outcomes

Primary

Measure	Time frame
The primary endpoint is quality of life and sexual health before the robot-assisted cystectomy and 3,6,9 and 12 months afterwards, as measured by numerical scores in the EORTC questionnaires.	—

Secondary

Measure	Time frame
The secondary endpoint is quality of life and sexual health before robot-assisted cystectomy and 3,6,9 and 12 months afterwards, assessed by numerical scores in the EORTC questionnaires in relation to the oncological characteristics of the patients, collected by internal data analysis, such as TNM status at the surgical resectate.	—

Countries

Germany

Contacts

Public ContactSeverin Rodler

Klinik für Urologie, UKSH, Campus Kiel

severin.rodler@uksh.de0431 500-24801

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 4, 2026