A Scalp Lotion Toimprove Sensitive Scalp Syndrome

Status Completed

Clinical Trial Summary

Overall, 100 Caucasian subjects participated in this 6-weeks lasting study, AC5+ was applied daily. All subjects had clinically confirmed mild to moderate alopecia and self-declared sensitive scalp. Instrumental assessments included Trans Epidermal Water Loss (TEWL), inflammation markers, clinical assessments included the severity of erythema, inflammation and greasiness. Subjective/Self assessments comprised the intensity of the scalp itch/pruritus and the evaluation of their head hair status (volume, abundance, strength). Same assessments were provided by the investigators.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT05630027
Study type	Observational
Source	Cosmetique Active International
Contact
Status	Completed
Phase
Start date	January 2, 2019
Completion date	June 30, 2020

View Details

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