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Hypotrichosis clinical trials

View clinical trials related to Hypotrichosis.

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NCT ID: NCT06376409 Recruiting - Hair Thinning Clinical Trials

Prospective Study of Nutraceutical Supplements to Support Hair Growth in Females

Start date: May 6, 2024
Phase: N/A
Study type: Interventional

A single site open label interventional study evaluating currently marketed hair supplements targeting the underlying root causes of thinning hair.

NCT ID: NCT06362941 Recruiting - Hair Thinning Clinical Trials

Evaluation of an Oral Hair Supplement to Improve Hair Strength and Support Growth in Women and Men

Start date: May 20, 2024
Phase: N/A
Study type: Interventional

A single-center, open-label, prospective study to demonstrate the efficacy of an oral supplement to improve the strength and support the growth of thinning hair in men and women with self-perceived hair thinning.

NCT ID: NCT06146166 Recruiting - Hair Thinning Clinical Trials

The Effects of an Oral Hair Supplement on Hair Density, Growth, and Microbiome

Start date: February 22, 2024
Phase: N/A
Study type: Interventional

The purpose of this study is to assess how an oral herbal supplement influences hair density, shine, growth, and microbiome.

NCT ID: NCT06010745 Recruiting - Hair Thinning Clinical Trials

Effectiveness of a Novel Dietary Ingredient on Hair Growth and Skin's Appearance

Start date: August 11, 2023
Phase: N/A
Study type: Interventional

The objective of this study is to assess the effectiveness of a novel dietary ingredient containing biotin and silicon for promoting hair growth and improving skin's appearance with six months of continuous daily usage among healthy adults.

NCT ID: NCT05790941 Recruiting - Hypotrichosis Clinical Trials

Proof of Concept Study of Latanoprost/Minoxidil (ANR-001.1) Topical Formulation

Start date: March 11, 2023
Phase: Early Phase 1
Study type: Interventional

Study to Evaluate the safety and efficacy of a Latanoprost/Minoxidil formulation vs. placebo for the treatment of hypotrichosis of the eyebrows.

NCT ID: NCT05723198 Recruiting - Skin Diseases Clinical Trials

A Study of Baricitinib (LY3009104) in Children From 6 Years to Less Than 18 Years of Age With Alopecia Areata

BRAVE-AA-PEDS
Start date: February 27, 2023
Phase: Phase 3
Study type: Interventional

The main purpose of this study is to determine the efficacy and safety of baricitinib for the treatment of severe or very severe alopecia areata (hair loss) in children from 6 years to less than 18 years of age. The study is divided into 4 periods, a 5-week Screening period, a 36-week Double-Blind Treatment Period, an approximately 2-year Long-term Extension Period, and a 4-week Post-treatment Follow-up period.

NCT ID: NCT04048031 Recruiting - Hair Thinning Clinical Trials

Efficacy and Safety of a Nutraceutical Supplement With Standardized Botanicals in Peri-menopausal and Menopausal Women With Thinning Hair

Start date: June 18, 2019
Phase: N/A
Study type: Interventional

NUTRAFOL® Women's Balance supplement is a novel nutraceutical supplement, scientifically formulated to specifically target the multiple underlying causes of hair loss and thinning in women. NUTRAFOL® Women's Balance capsules are comprised of primary and secondary ingredients, designed to restore hair health from the inside out. In addition to the necessary vitamins, minerals, proteins to support the nutritional needs of hair, it also contains nutraceutical-grade botanical bioactives that are standardized and clinically tested. The formulation leverages the multidimensional properties of power plants, which possess a full spectrum of phytochemicals with innate capacities to work in synergy with each other to fulfill their specific therapeutic roles. Using the latest biotechnology, these ingredients are bio-optimized and standardized, extracted with patented methods that preserve their bioactive integrity and made more bio-available and bio-absorbable via specific patented technologies. Ingestion of NUTRAFOL® Women's Balance supplement over a six (6) month period will strengthen and promote the growth of hairs in perimenopausal, menopausal, and post-menopausal female subjects with self-perceived thinning hair when compared to baseline and those using the placebo tablet, with further improvement during the subsequent six (6) month open-label extension period.

NCT ID: NCT04018859 Recruiting - Clinical trials for Eyebrow Hypotrichosis

Platelet-rich Plasma for Eyebrows

Start date: September 25, 2019
Phase: Phase 2
Study type: Interventional

The purpose of this study is to evaluate the effect of autologous platelet-rich plasma (PRP) in the treatment of mild to moderate eyebrow hypotrichosis. This is a randomized clinical trial to evaluate the effect of autologous platelet rich plasma in subjects with mild to moderate eyebrow hypotrichosis. Approximately 40 subjects will be randomized to receive platelet-rich plasma (PRP) or saline injections. The study is designed as an 9-month study. This study was a pilot study designed to determine feasibility of this procedure. Subjects currently living in the Chicago metropolitan area and meet inclusion/exclusion criteria will be considered for enrollment.