Clinical Trials Directory

Trials / Completed

CompletedNCT05630027

A Scalp Lotion Toimprove Sensitive Scalp Syndrome

Soothing and Anti-hair Loss Activity of a Scalp Lotion Containing Piroctone Olamine, 2,4 Diaminopyrimidine Oxide and Vichy Mineralizing Water

Status
Completed
Phase
Study type
Observational
Enrollment
100 (actual)
Sponsor
Cosmetique Active International · Industry
Sex
Age
Healthy volunteers

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.

Conditions

Interventions

TypeNameDescription
OTHERPiroctone Olamine (PO), 2,4 Diaminopyrimidine oxide (2.4 DA) and Vichy mineralizing waterobservational, prospective study

Timeline

Start date
2019-01-02
Primary completion
2020-06-30
Completion
2020-06-30
First posted
2022-11-29
Last updated
2022-11-29

Locations

1 site across 1 country: France

Source: ClinicalTrials.gov record NCT05630027. Inclusion in this directory is not an endorsement.

A Scalp Lotion Toimprove Sensitive Scalp Syndrome (NCT05630027) · Clinical Trials Directory