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Androgenetic Alopecia clinical trials

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NCT ID: NCT03495817 Recruiting - Clinical trials for Androgenetic Alopecia

A Study in Male and Female Subjects With Androgenetic Alopecia Treated With ATI-50002 Topical Solution

Start date: March 22, 2018
Phase: Phase 2
Study type: Interventional

Open label study to assess safety, tolerability, and efficacy of ATI-50002 in male and female subjects with androgenetic alopecia.

NCT ID: NCT03394235 Recruiting - Clinical trials for Androgenetic Alopecia

Optimizing Parameters for Long-pulsed Nd:YAG Laser for Reducing Hair Shaft Diameter

Start date: February 2, 2018
Phase: N/A
Study type: Interventional

This study evaluates the optimizing parameters of long pulse Nd:YAG Laser for reducing the size of hair shaft diameter of the donor for hair transplantation. All participants will receive long-pulsed Nd-YAG laser treatments with three different parameters at the occipital area.

NCT ID: NCT03388840 Recruiting - Clinical trials for Androgenetic Alopecia

Adipose Derived Stem Cells Versus Platelet Rich Plasma on Follicular Unit Extraction

Start date: January 15, 2018
Phase: Phase 4
Study type: Interventional

Androgenetic alopecia is the most common type of alopecia in both men and women. About 80 % of Caucasian men and 40-50 % of Caucasian women are affected by androgenetic alopecia. The psychological impact of hair loss due to Androgenetic alopecia can be profound.

NCT ID: NCT03376581 Active, not recruiting - Clinical trials for Androgenetic Alopecia

The Utility of Platelet Rich Plasma in Hair Loss

Start date: November 28, 2017
Phase: Early Phase 1
Study type: Interventional

Platelet rich plasma (PRP) is an autologous preparation of human plasma with high concentration of platelets. Platelets release numerous growth factors, which stimulate cell proliferation and differentiation. The purpose of this research is to investigate the potential of PRP injection for treatment of hair loss. Clinical outcomes will be assessed by noninvasive techniques including dermoscopy, multiphoton microscopy, optical coherence tomography, optical Doppler tomography and multispectral imaging.

NCT ID: NCT03048461 Not yet recruiting - Clinical trials for Androgenetic Alopecia

The Effect of Platelet-rich Plasma in Subjects With Androgenetic Alopecia

Start date: May 2018
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 androgenetic alopecia. This is a randomized clinical trial to evaluate the effect of autologous platelet rich plasma in subjects with moderate androgenetic alopecia. Approximately 30 subjects will be randomized into the study. The study is designed as an 18-month study consisting of 2 phases. 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.

NCT ID: NCT02999737 Active, not recruiting - Clinical trials for Androgenetic Alopecia

Comparing Different Platelet Rich Plasma (PRP) Treatment Regimens for Management of Androgenic Alopecia

Start date: November 2016
Phase: Phase 4
Study type: Interventional

The injection of autologous platelet rich plasma (PRP) is a relatively novel therapy, generating interest across a wide variety of medical specialties, such as orthopedics, dentistry, ophthalmology, and dermatology. Several recently published studies have demonstrated efficacy in treating androgenetic alopecia (aka male or female patterned hair loss), but each varies in the treatment protocol, and there is no evidence-based data to date guiding the dosing parameters of and intervals between injection sessions. We propose a single-center, single-blinded randomized pilot trial to investigate the most beneficial number and frequency ('schedule') of necessary PRP injections in men and women with androgenetic alopecia.

NCT ID: NCT02848300 Completed - Clinical trials for Androgenetic Alopecia

Local Pharmacokinetics and Tolerability of Bimatoprost Applied to the Scalp of Male Patients With Androgenetic Alopecia

Start date: July 2016
Phase: Phase 1
Study type: Interventional

This study will evaluate the skin pharmacokinetics and tolerability of bimatoprost Formulation A and Formulation B following 14 days of once daily topical administration in male participants with androgenetic alopecia (AGA).

NCT ID: NCT02791243 Completed - Clinical trials for Androgenetic Alopecia

Photosensitization Study in Androgenetic Alopecia

Start date: May 9, 2016
Phase: Phase 1
Study type: Interventional

This study evaluates the potential for induction of photosensitization by P-3074 0.25% finasteride cutaneous solution compared to that of placebo vehicle cutaneous solution and a negative control (0.9% sodium chloride, NaCl)

NCT ID: NCT02729415 Recruiting - Clinical trials for Androgenetic Alopecia

Point-of-Care Adipose-derived Cells for Hair Growth

ASVF-2016
Start date: October 2016
Phase: Early Phase 1
Study type: Interventional

Androgenetic alopecia (AGA) is the most common form of hair loss and affects 50% and 23% of Caucasian men and women, respectively, over the age of 50. The percentage of men and women affected over the age of 70 increases to 80% and 60% of Caucasian men and women, respectively. Although alopecia is considered a minor dermatologic condition, it is seen as a serious condition with major life consequences by those with alopecia and has been associated with increased incidence of myocardial infarction, hypertension and hypercholesterolaemia. Androgenetic alopecia is associated with feelings of anxiety, depression and various personality disorders among men and women due to physical appearance. Depression, anxiety, aggressiveness, impaired quality of life and social inadequacy have been documented. The presence of alopecia in women is particularly stressful. ADSCs (Adipose Derived Stromal Cells), also called Stromal Vascular Fraction (SVF) cells, include regenerative cell populations derived from adipose tissue and thus are potentially important to multiple disease processes and therapeutic applications for the repair and regeneration of acute and chronically damaged tissues. It has been postulated that SVF cells may promote hair regeneration by increasing the hair-inducing ability of dermal papillae (DP) cells. The general objective of this study is to conduct a safety and feasibility study of a single injection of autologous adipose-derived SVF cells for the treatment of alopecia.

NCT ID: NCT02626780 Completed - Clinical trials for Androgenetic Alopecia

Adipose-derived SVF for Treatment of Alopecia

Start date: December 2015
Phase: N/A
Study type: Interventional

The general objective of this study is to conduct a safety and feasibility study of a single injection of autologous adipose-derived SVF for the treatment of alopecia.