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Clinical Trial Summary

In the course of this clinical trial, it was shown that the use of Granudacyn/VERIFORTE med wound irrigation solution in the course of adjuvant therapy supports wound healing through mechanical irrigation and moistening of the wound. No risks have been reported. The benefits of using Granudacyn/VERIFORTE med wound irrigation solution therefore outweigh the potential risks.


Clinical Trial Description

Aim of this clinical trial was to collect clinical data on the performance and safety of the use of Granudacyn/VERIFORTE med as a wound irrigation solution, for cleansing and irrigation of acute, chronic or contaminated wounds. The evaluation of the safety of the use of Granudacyn/VERIFORTE med wound irrigation solution within the scope of use was based on the frequency of adverse events (AEs) and, in particular, treatment-emergent adverse events (ADEs). Study Design: - Open-label, retrospective, monocentric, PMCF, non-interventional, observational study. - One treatment group (single arm): All subjects participating in the study will be treated with Granudacyn/VERIFORTE med wound irrigation solution. - The study will be conducted in Austria. The participating trial centre is in Lower Austria: WPM Ges.m.b.H ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06083740
Study type Observational
Source P.G.F. Industry Solutions GmbH
Contact
Status Completed
Phase
Start date November 1, 2022
Completion date June 1, 2023

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