DSD de Luxe / Clinical research
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Our clinical evaluation of a three-step anti-hair-loss routine in volunteers with androgenetic alopecia, under dermatological supervision.
Participants
25 volunteers, ages 23–68, with androgenetic alopecia
Duration
Approximately 12 weeks (19 Jan – 12 Apr 2016)
Method
Dermatological supervision; Visioscan® VC 98
Measured outcomes
Key study results
These percentages are presented in our study under “Overall evaluation.” The study summary does not define them as measured percentage changes in hair count, growth rate or density.
Study photographs
Images from the study
Study details
Clinical study report
Our anti-hair-loss efficacy study followed 25 volunteers aged 23–68 with androgenetic alopecia from 19 January to 12 April 2016. The treatment was evaluated under dermatological supervision using the Visioscan® VC 98 imaging system.
Overall evaluation
Alongside the three results highlighted above, the evaluation recorded 100% for healthier-looking hair.
The study presents its four percentages as an overall evaluation. It does not specify whether these percentages reflect participant assessments or direct measurements of changes in hair count, hair-growth rate or density.
Tested products
Products used in this study
Results reflect the participants and conditions of each study. Individual outcomes may vary.