The goal of this study is to determine how safe and effective it is to improve hair growth using an active gummy treatment in women with self-perceived thinning hair. The main aims of this trial are: 1. To confirm using photographic analysis, changes in the quality, volume, and thickness of hair. 2. To gauge patient satisfaction with hair changes and application process. 3. Monitor and report any adverse events associated with the daily intake of Xtressé Participants who qualify will complete 5 visits after voluntary consent has been given. Participants will be given a 30-day supply of the gummies at each visit over a 4-month period. Photographs and scalp analysis will be performed at each visit to measure changes in hair volume, thickness, and growth.
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Hair Density Changes measured by SOCAi
Timeframe: From enrollment to the end of the study at 4 months
Within-subject increase in hair density assessed via Canfield HairMetrix® Phototrichogram Analysis
Timeframe: From enrollment to the end of treatment at 4 months
Within-subject increase in hair thickness assessed via Canfield HairMetrix® Phototrichogram Analysis
Timeframe: From enrollment to the end of treatment at 4 months