Overview
The trial aims to investigate the effect of a topical application of a medical device based on inositol in recovering breast pain
Description
The present study enrolled patients with breast pain (measured through the VAS) aiming to evaluate the improvement of the pain after the local treatment
Eligibility
Inclusion Criteria:
- Women aged between 18 and 70 years
- Women who underwent breast surgery at least 15 days prior
- Women experiencing breast pain associated with the surgical wound
Exclusion Criteria:
- Women under the age of 18
- Ongoing systemic and/or local pain therapy
- Pregnant women