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Clinical Trial Summary

The main objective of this study is to estimate the change in the relative numbers of commensal or low virulence potential bacteria before and after one session TDP.


Clinical Trial Description

The secondary objectives of this study are:

- To estimate changes in several microbiological parameters over three time periods (before treatment, after applying the Metvixia® and after irradiation during a single TDP session).

- Describe the evolution of the size and appearance of the wound 7d after the start of treatment

- Describe the potential adverse events associated with a TDP session ;


Study Design

Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


NCT number NCT02392390
Study type Interventional
Source Centre Hospitalier Universitaire de Nimes
Contact
Status Completed
Phase N/A
Start date October 2015
Completion date March 2016

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