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Hair Loss clinical trials

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NCT ID: NCT04558242 Recruiting - Clinical trials for Androgenetic Alopecia

Low Level Light Device as a Primary Therapy for Androgenetic Alopecia

Start date: August 1, 2020
Phase: N/A
Study type: Interventional

The purpose of this research is to study the safety and effectiveness of a light therapy device for human hair growth. This device, called the GENIX, is a type of cold, or non-heat producing light emitting diode (LED) that will emit light on the hair growth cells within and around the hair follicle. When these cells do not function properly, one may experience common problems such as baldness and thinning or brittle hair. The application of a special category of low-level non-laser light to be studied in the project may cause an increase in essential nutrients to the damaged hair follicles and skin cells, leading to a reduction in hair loss and in some cases, possibly leading to re-growth.

NCT ID: NCT04554732 Completed - Alopecia Clinical Trials

Keratinocyte Growth Factor- Hair Serum for the Prevention of Chemotherapy Induced Alopecia

Start date: April 27, 2020
Phase: Early Phase 1
Study type: Interventional

Primary aim is to provide a preliminary assessment of the efficacy of the investigational topical formula, KGF-HS, as a prophylactic treatment for chemotherapy induced alopecia. Hypothesis: KGF-HS will result in less than 50% hair loss by the end of 4 cycles of chemotherapy. The investigators will evaluate hair loss using the CTCAE (Common Terminology Criteria for Adverse Events) v4.0 alopecia grading scale.

NCT ID: NCT04379583 Withdrawn - Clinical trials for Androgenetic Alopecia

HairDx Analytical Validation Study

Start date: June 15, 2020
Phase:
Study type: Observational

The HairDx Test reports genetic variants associated with the development of FPHL.

NCT ID: NCT04298840 Withdrawn - Hair Loss Clinical Trials

Influence of Creatine Monohydrate Supplementation on Androgens and Global Hair Assessments

Start date: April 2020
Phase: N/A
Study type: Interventional

This study is a randomized, double-blind, placebo-controlled trial examining the effects of creatine monohydrate supplementation on androgens and hair loss in free-living adult males. Participants will complete 6 months of supplementation of 5 grams per day of creatine monohydrate while following their normal lifestyle practices. At baseline and six months after study initiation, participants will complete laboratory assessments. These assessments will include a standard blood draw for evaluation of total testosterone (T), free T, dihydrotestosterone (DHT), and DHT:T ratios in the blood, as well as global photography and questionnaires to evaluate hair loss. This study will examine the claim that creatine increases DHT concentrations and and DHT:T ratio, as well as provide novel data regarding whether creatine promotes hair loss.

NCT ID: NCT04249128 Completed - Skin Aging Clinical Trials

Nourishing Hair, Skin & Nails Supplement Study (Derm Aid)

Start date: January 15, 2020
Phase: Phase 3
Study type: Interventional

A 90 day eight arm virtual interventional study looking at the impact of various supplement formulations for improves in hair, skin & nail health via self report, and dermatology assessment via remote dermatologist assessment.

NCT ID: NCT03709563 Terminated - Hair Loss Clinical Trials

Oral Nutraceutical Supplement With Standardized Botanicals in Males With Self-Perceived Thinning Hair and Loss

Start date: October 15, 2018
Phase: N/A
Study type: Interventional

Hair loss study in men with self-perceived thinning hair and loss

NCT ID: NCT03652701 Withdrawn - Hair Loss Clinical Trials

Hair Up Prospective Study

Start date: April 1, 2019
Phase: N/A
Study type: Interventional

The objective of this study is to assess the performance of Hair Up on female pattern hair shedding and regrowth. 58 adult female patients suffering from hair loss will be evaluated in a single center prospective study

NCT ID: NCT03351322 Completed - Alopecia Clinical Trials

ENERGI-F701 for Female Hair Loss Treatment

Start date: May 23, 2018
Phase: Phase 2
Study type: Interventional

The objective of this study is to evaluate the efficacy and safety of ENERGI-F701 Solution in female subjects with hair loss.

NCT ID: NCT03155958 Not yet recruiting - Hair Loss Clinical Trials

Ocular Finding in Alopecia Areata

Start date: July 1, 2017
Phase: N/A
Study type: Observational

Alopecia areata (AA) is a common, idiopathic and sometimes recurrent non-scarring type of hair loss. Several etiological factors, including psychological, trauma-related, genetic and autoimmune factors have been considered as possible etiological factors . A T cell-mediated autoimmune mechanism in genetically vulnerable individuals is the most acceptable etiology. Alopecia areata presents clinically with well demarcated patches of non cicatricial hair loss in any hair bearing area with no remarkable gender preference. Although AA may occur at any age, incidence is high among younger age groups. In fact, it is the most common form of alopecia seen in children. Various clinical patterns of alopecia have been described as patchy, diffuse, reticulate, ophiasis and ophiasis inversus. Depending on the extent of hair loss, it can be classified into alopecia subtotalis, alopecia totalis (complete loss of scalp hair), and alopecia universalis (complete loss of body hair). National Alopecia Areata Foundation has devised "Severity of Alopecia Tool Score" (SALT score) as a measure of disease severity. Scalp is divided into 4 areas, namely, Vertex-40% of scalp surface area; right and left profiles-18% each and posterior scalp aspect-24%. SALT score is the sum of percentage of hair loss in the above mentioned areas.

NCT ID: NCT03052413 Completed - Hair Loss Clinical Trials

Study to Evaluate a Nutraceutical Supplement for Treatment of Hair Loss and Thinning in Females

Start date: December 2016
Phase: N/A
Study type: Interventional

The objective of this study is to assess the safety and effectiveness of a nutraceutical supplement for the treatment of hair loss and thinning in females over the course of six months of continuous daily use.