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Clinical Trials/DRKS00031191
DRKS00031191
Recruiting
N/A

Prospective observational study for the evaluation of recurrences/primary hernias and technical or postoperative complications in the context of surgical practice for the treatment/prevention of abdominal wall, inguinal, diaphragm and parastomal hernias with DynaMesh® mesh implants - Pro-DMH-Register

FEG Textiltechnik Forschungs- und Entwicklungsgesellschaft mbH0 sites120 target enrollmentFebruary 7, 2023

Overview

Phase
N/A
Intervention
Not specified
Conditions
Epigastric Hernias, Hiatus Hernias, Prevention and Treatment of Incisional Hernias, Inguinal Hernias, Umbilical Hernias, Treatment and Prevention of Parastomal Hernias
Sponsor
FEG Textiltechnik Forschungs- und Entwicklungsgesellschaft mbH
Enrollment
120
Status
Recruiting
Last Updated
last year

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
February 7, 2023
End Date
TBD
Last Updated
last year
Study Type
Observational
Sex
All

Investigators

Sponsor
FEG Textiltechnik Forschungs- und Entwicklungsgesellschaft mbH

Eligibility Criteria

Inclusion Criteria

  • Indication for the treatment/prevention of an abdominal wall, inguinal, diaphragmatic and/or parastomal hernia with a corresponding DynaMesh® mesh implant

Exclusion Criteria

  • As this is an observation of routine clinical practice, only patients who do not meet the inclusion criteria are excluded.

Outcomes

Primary Outcomes

Not specified

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