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Mechanical Intervention on the Scalp Microbiome: Setting the Stage for the Future Management of Cicatricial Alopecias

Megadott ok: There was only one participant

A legfontosabb adatok

Hol
Minneapolis (Egyesült Államok)A helyszín megnézése

Helyszínek itt: Egyesült Államok

  • University of MinnesotaMinneapolis, Egyesült ÁllamokNo longer taking part

A vizsgálat adatai

Ki végzi
University of Minnesota
Azonosító
NCT06357169
A regiszteradat frissítve
2025. február 12.
Eredeti leírás
The objective of this study is to assess the effect of standardized scalp care, specifically mechanical cleansing with the Venus Glow™ Device and water, on the scalp microbiome. This study also seeks to characterize the microbiome of the normal, healthy scalp, thereby providing a baseline for which the scalp affected by hair and scalp disease can be compared.A teljes eredeti leírásKevesebb

Effect of Mechanical Intervention on the Scalp Microbiome: Setting the Stage for the Future Management of Cicatricial Alopecias

The objective of this study is to assess the effect of standardized scalp care, specifically mechanical cleansing with the Venus Glow™ Device and water, on the scalp microbiome. This study also seeks to characterize the microbiome of the normal, healthy scalp, thereby providing a baseline for which the scalp affected by hair and scalp disease can be compared.

Bevonási feltételek: All individuals between 18-35 years of age; Ability to understand study procedures and to comply with them.

Kizáró feltételek: Using oral or topical antimicrobial medication 4 weeks prior to their baseline visit or in the duration of the study; Current scalp or hair disease diagnosis; Current clinical condition that, in the opinion of the site investigator, would interfere with adherence to study requirements; Non-English speakers; Exclusion related to pregnancy, lactation, or has plans to become pregnant over the course of the study, Based on self-report from the participant; Inability or unwillingness of individual to give written informed consent.

ClinicalTrials.gov NCT06357169