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Clinical Trial Summary

The objective of this clinical trial is to assess the effectiveness of acetic acid in patients suffering from chronic cutaneous ulcers with biofilm. The primary question it seeks to address is whether acetic acid (as a 2% topical solution) is superior to the current standard treatment for chronic cutaneous ulcers with biofilm at our center (Prontosan®). Participants will be randomly assigned to receive either the acetic acid solution treatment or the standard current treatment.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT06297967
Study type Interventional
Source Consorci Sanitari de l'Alt Penedès i Garraf
Contact Marta De Vicente
Phone +34 9389316161
Email mdevicente@csapg.cat
Status Not yet recruiting
Phase Phase 3
Start date April 2024
Completion date June 2026

See also
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