Monocentric cohort study to evaluate the artificial urinary sphincter Victo and Victo+

Monocentric cohort study to evaluate the artificial urinary sphincter Victo and Victo+ - Vena

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

DRKS

Registry ID

DRKS00018990

Enrollment

Registered

2020-01-31

Start date

2020-01-30

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

male stress urinary incontinence N39.3

Interventions

Group 1: Male patients, who received an artificial urinary sphincter Victo or Victo+ of the third generation will be retrospectively evaluated concerning functional outcome and complication rates. F

Eligibility

Sex/Gender

Male

Age

18 Years to No maximum

Inclusion criteria

Inclusion criteria: male patients with a age > 18 years Male Patients who received a Victo or Victo+ of the third generation for the treatment of male urinary stress incontinence

Exclusion criteria

Exclusion criteria: missing signed informed consent

Design outcomes

Primary

Measure	Time frame
Urinary continence which is defined with the usage of 0 to 1 pad/day	—

Secondary

Measure	Time frame
Complication rates, Revision- and explantation free survival, time period of being continent, 24h pad test, validated questionare PGI-I, ICIQ-SF and I-QoL	—

Countries

Austria

Contacts

Public ContactGhazal Amelie

Klinik für Urologie Landesklinikum Korneuburg

ghazal.ameli@korneuburg.lknoe.at+43 2262 9004 5740

Outcome results

None listed

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