Efficacy and Safety of a Dietary Supplement on Hair Growth and Hair Health in Female With Acute T… (NCT06545552) | Clinical Trial Compass
CompletedNot Applicable
Efficacy and Safety of a Dietary Supplement on Hair Growth and Hair Health in Female With Acute Telogen Effluvium
Italy66 participantsStarted 2024-09-30
Plain-language summary
The study is aimed to assess the efficacy of a food supplement in reducing hair loss and accelerating the physiological growth in terms of elongation in female subjects showing acute telogen effluvium. Moreover, the efficacy of the product in increasing hair elasticity, thickness and brightness will be assess.
In order to reach this goal a randomized, double-blind, placebo controlled, parallel group (2 arms), clinical trial is carried out on 66 healthy female subjects aged between 18 and 52 years old, showing acute telogen effluvium will be enrolled.
Who can participate
Age range18 Years – 52 Years
SexFEMALE
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Inclusion Criteria:
* Good general health
* Caucasian ethnicity
* All hair type included
* Transient acute telogen effluvium (duration less than 6 months) due to fatigue, seasonal change, deficiency of vitamins and minerals, stress, change or imbalance of normal daily routing, or emotional stress
* Subjects having a positive pull test result
* Subjects with minimum hair length of 6/7 cm
* Subjects who stopped any anti hair loss treatment at least 3 months prior the study
* Subjects agreeing not to take any treatment (oral or topic) able to interfere with the hair growth, diameter or fall during the whole study duration
* Willingness not to dye/blench hair during the 2 weeks preceding each visit
* Willingness not to cut hair for all the study length
* Subjects registered with health social security or health social insurance
* Subjects having signed their written Informed Consent form (ICF) and Privacy Policy for their participation in the study and a photograph authorization
* Subjects able to understand the language used in the investigation centre and the information given
* Subjects able to comply with the protocol and follow protocol constraints and specific requirements
* Willingness to use during all the study period only the product to be tested
* Willingness not to use similar products that could interfere with the product to be tested
* Willingness to not vary the normal daily routine (i.e. lifestyle, physical activity, diet etc.)
* Subjects under effective contrace…