Biofilm Correlation & Validation

Clinical Trial Summary

This is a prospective, single-blind, controlled trial. There are two arms and 20 patients with acute or chronic wounds with clinical suspicion of biofilm (CSB+/CSB-) are allocated in each arm. The primary objective is to evaluate the diagnostic accuracy of MolecuLight fluorescence in identifying biofilm as validated by gold standard SEM imaging.

See also
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NCT number	NCT05196880
Study type	Observational [Patient Registry]
Source	MolecuLight Inc.
Contact
Status	Completed
Phase
Start date	February 15, 2022
Completion date	November 8, 2023

Biofilm Correlation and Validation

Clinical Trial Summary

Clinical Trial Description

Study Design

Related Conditions & MeSH terms