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Adjustable Artificial Sphincter Victo in the Treatment of Male Incontinence Due to Prostate Surgery

NCT06239909 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 150

Last updated 2024-02-02

No results posted yet for this study

Summary

The aim of this prospective academic research study is to evaluate the efficacy and safety of the Victo adjustable artificial sphincter in the treatment of male patients with urinary incontinence due to prostate surgery.

Conditions

Interventions

OTHER

24-h pad-weight test

The patients will be asked to perform the 24-h pad-weight test

OTHER

Patient Global Impression - Improvement Questionnaire

The patient-reported outcome, as measured by PGI-I (Patient Global Impression - Improvement Questionnaire)

Sponsors & Collaborators

  • University Hospital Ostrava

    lead OTHER

Principal Investigators

  • Jan Krhut, prof.,MD, PhD · University Hospital Ostrava

Eligibility

Min Age
18 Years
Sex
MALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2018-05-01
Primary Completion
2026-12-31
Completion
2026-12-31

Countries

  • Czechia

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06239909 on ClinicalTrials.gov