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EUREKA study – the evaluation of real-life use of a biophotonic system in chronic wound management: an interim analysis

OBJECTIVE: Interest has grown regarding photobiomodulation (PBM) with low-level light therapy, which has been shown to positively affect the stages of the wound healing process. In a real-life context clinical setting, the objective of the EUREKA study was to investigate efficacy, safety, and qualit...

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Autores principales: Romanelli, Marco, Piaggesi, Alberto, Scapagnini, Giovanni, Dini, Valentina, Janowska, Agata, Iacopi, Elisabetta, Scarpa, Carlotta, Fauverghe, Stéphane, Bassetto, Franco
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5729886/
https://www.ncbi.nlm.nih.gov/pubmed/29270004
http://dx.doi.org/10.2147/DDDT.S142580
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author Romanelli, Marco
Piaggesi, Alberto
Scapagnini, Giovanni
Dini, Valentina
Janowska, Agata
Iacopi, Elisabetta
Scarpa, Carlotta
Fauverghe, Stéphane
Bassetto, Franco
author_facet Romanelli, Marco
Piaggesi, Alberto
Scapagnini, Giovanni
Dini, Valentina
Janowska, Agata
Iacopi, Elisabetta
Scarpa, Carlotta
Fauverghe, Stéphane
Bassetto, Franco
author_sort Romanelli, Marco
collection PubMed
description OBJECTIVE: Interest has grown regarding photobiomodulation (PBM) with low-level light therapy, which has been shown to positively affect the stages of the wound healing process. In a real-life context clinical setting, the objective of the EUREKA study was to investigate efficacy, safety, and quality of life associated with the use of a BioPhotonic gel (LumiHeal™) in the treatment of chronic wounds such as venous leg ulcers (VLUs), diabetic foot ulcers (DFUs), and pressure ulcers (PUs). This BioPhotonic gel represents a new, first-in-class emission spectrum of light, including fluorescence, to induce PBM and modulate healing. DESIGN: The multicenter, prospective, interventional, uncontrolled, open-label study enrolled 100 patients in 12 wound centers in Italy. We performed an early interim analysis based on the first 33 subjects (13 VLU, 17 DFU, 3 PU) in seven centers who completed the study. MAIN RESULTS: Seventeen patients (52%) achieved total wound closure (full re-epithelialization for 2 weeks) during the study period. Two patients (6%) were considered “almost closed” (decrease of the wound area of more than 90% at study end) and three others (9%) were considered “ready for skin grafting”. No related serious adverse events were observed, and the compliance was excellent. After the treatment, the average time to “pain-free” was 11.9 days in the VLU group. Quality of life was improved with overall increase of 26.4% of the total score (Cardiff Wound Impact Schedule, p=0.001). CONCLUSION: The study revealed a positive efficacy profile of the BioPhotonic gel in promoting wound healing and reactivating the healing process in different types of chronic, hard-to-heal wounds. The treatment was shown to be safe and well tolerated by the patients, and a reduction of pain perception was also detected during the treatment period. The improvement of the quality of life was accompanied by a high level of clinician satisfaction.
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spelling pubmed-57298862017-12-21 EUREKA study – the evaluation of real-life use of a biophotonic system in chronic wound management: an interim analysis Romanelli, Marco Piaggesi, Alberto Scapagnini, Giovanni Dini, Valentina Janowska, Agata Iacopi, Elisabetta Scarpa, Carlotta Fauverghe, Stéphane Bassetto, Franco Drug Des Devel Ther Clinical Trial Report OBJECTIVE: Interest has grown regarding photobiomodulation (PBM) with low-level light therapy, which has been shown to positively affect the stages of the wound healing process. In a real-life context clinical setting, the objective of the EUREKA study was to investigate efficacy, safety, and quality of life associated with the use of a BioPhotonic gel (LumiHeal™) in the treatment of chronic wounds such as venous leg ulcers (VLUs), diabetic foot ulcers (DFUs), and pressure ulcers (PUs). This BioPhotonic gel represents a new, first-in-class emission spectrum of light, including fluorescence, to induce PBM and modulate healing. DESIGN: The multicenter, prospective, interventional, uncontrolled, open-label study enrolled 100 patients in 12 wound centers in Italy. We performed an early interim analysis based on the first 33 subjects (13 VLU, 17 DFU, 3 PU) in seven centers who completed the study. MAIN RESULTS: Seventeen patients (52%) achieved total wound closure (full re-epithelialization for 2 weeks) during the study period. Two patients (6%) were considered “almost closed” (decrease of the wound area of more than 90% at study end) and three others (9%) were considered “ready for skin grafting”. No related serious adverse events were observed, and the compliance was excellent. After the treatment, the average time to “pain-free” was 11.9 days in the VLU group. Quality of life was improved with overall increase of 26.4% of the total score (Cardiff Wound Impact Schedule, p=0.001). CONCLUSION: The study revealed a positive efficacy profile of the BioPhotonic gel in promoting wound healing and reactivating the healing process in different types of chronic, hard-to-heal wounds. The treatment was shown to be safe and well tolerated by the patients, and a reduction of pain perception was also detected during the treatment period. The improvement of the quality of life was accompanied by a high level of clinician satisfaction. Dove Medical Press 2017-12-11 /pmc/articles/PMC5729886/ /pubmed/29270004 http://dx.doi.org/10.2147/DDDT.S142580 Text en © 2017 Romanelli et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed.
spellingShingle Clinical Trial Report
Romanelli, Marco
Piaggesi, Alberto
Scapagnini, Giovanni
Dini, Valentina
Janowska, Agata
Iacopi, Elisabetta
Scarpa, Carlotta
Fauverghe, Stéphane
Bassetto, Franco
EUREKA study – the evaluation of real-life use of a biophotonic system in chronic wound management: an interim analysis
title EUREKA study – the evaluation of real-life use of a biophotonic system in chronic wound management: an interim analysis
title_full EUREKA study – the evaluation of real-life use of a biophotonic system in chronic wound management: an interim analysis
title_fullStr EUREKA study – the evaluation of real-life use of a biophotonic system in chronic wound management: an interim analysis
title_full_unstemmed EUREKA study – the evaluation of real-life use of a biophotonic system in chronic wound management: an interim analysis
title_short EUREKA study – the evaluation of real-life use of a biophotonic system in chronic wound management: an interim analysis
title_sort eureka study – the evaluation of real-life use of a biophotonic system in chronic wound management: an interim analysis
topic Clinical Trial Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5729886/
https://www.ncbi.nlm.nih.gov/pubmed/29270004
http://dx.doi.org/10.2147/DDDT.S142580
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