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Retrospective observational study of the safety and performance of the DynaMesh® PRM implant for the treatment of male stress urinary incontinence

Retrospective observational study of the safety and performance of the DynaMesh® PRM implant for the treatment of male stress urinary incontinence - Retro-AWB-PRM

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
DRKS
Registry ID
DRKS00031544
Enrollment
30
Registered
2023-03-23
Start date
2022-09-15
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

N39.4

Interventions

Group 1: Patients who underwent surgical treatment of stress incontinence using a DynaMesh®-PRM/ -PRM visible mesh implant at the Vivantes Klinikum am Urban between July 2017 and October 2020

Sponsors

FEG Textiltechnik Forschungs- und Entwicklungsgesellschaft mbH
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: All patients who underwent surgical treatment of stress incontinence using a DynaMesh®-PRM/ -PRM visible mesh implant at the Vivantes Klinikum am Urban between July 2017 and October 2020 are included.

Exclusion criteria

Exclusion criteria: Since this is an observational study within the framework of usual treatment practice, there are no study-related exclusion criteria.

Design outcomes

Primary

MeasureTime frame
This observational study primarily serves to assess the performance of the product DynaMesh-PRM (visible) Recurrent incontinence and reoperation if recurrence to assess product performance—

Secondary

MeasureTime frame
The secondary endpoints serve to assess the safety of the product DynaMesh-PRM (visible). Peri- and postoperative complications and follow-up data to assess safety—

Countries

Germany

Contacts

Public ContactTobias Pottek

Klinik für Urologie, Vivantes Klinikum Am Urban

tobias.pottek@vivantes.de+49 (0)30 130 22 6303

Outcome results

None listed

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