Hair Loss

8

Review clinical trials related to Hair Loss. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Not yet recruiting

Gut Microbiota and Trichoscopic Changes in Women With Telogen Effluvium on a Multifactorial Drinkable Nutraceutical: A Retrospective Observational Study

Telogen effluvium (TE) is a common cause of diffuse, non-scarring hair shedding in women. It is often triggered by physiological stress, nutritional deficiencies, illness or hormonal changes. There is growing interest in the role of the gut microbiota in hair health, through its effects on nutrient absorption, immune regulation and systemic inflammation (the so-called gut-skin axis). However, data on gut microbiota in women with TE are still scarce. This retrospective observational study will review the medical records of premenopausal women diagnosed with TE who received a multifactorial drinkable nutraceutical as part of routine clinical care at 2 clinics between January 2025 and July 2025. The study has two aims: 1. To describe the gut microbiota profile of these women at baseline \[and after 6 months\], as assessed by \[stool analysis method\]. 2. To describe changes in trichoscopic parameters, over 6 months of supplementation \[and to explore whether baseline microbiota features are associated with these changes\]. The study does not assign any intervention: all data were collected during standard clinical practice. Its findings are intended to generate hypotheses for future controlled studies.

Participants needed: 30
Trial details
Age: 18-40Biological sex: FemaleType: ObservationalSponsor: Olistic Research Labs S.L.Updated: Oct 9, 2026Locations: 2
Eligibility criteria

Women aged 18-40 years. [+3]

Moderate or severe irritable bowel syndrome (IBS). [+9]

Status: Recruiting

Dual Modality Treatment of Androgenic Alopecia With KeraFactor® Solution and Revian® LED Light Therapy

This single-center, prospective, randomized, placebo-controlled interventional study will evaluate the safety and efficacy of KeraFactor scalp-stimulating solution and the Revian Red wireless smart cap, alone and in combination, for the treatment of female androgenic alopecia. Forty female subjects aged 35 to 55 with clinically diagnosed androgenic alopecia will be randomized into four treatment arms and followed for 24 weeks. The primary objective is to determine whether combination therapy produces greater improvement in hair growth from baseline to 6 months compared with solution alone, device alone, or placebo. Secondary outcomes include changes in hair density, hair fiber diameter, interfollicular distance, terminal-to-vellus hair ratio, patient satisfaction, and safety/tolerability.

Participants needed: 40
Trial details
Age: 35-55Biological sex: FemaleType: InterventionalSponsor: K. Kay Durairaj, MD, FACS, A Medical CorporationUpdated: Sep 9, 2026Locations: 1
Eligibility criteria

Female participants aged 35 to 55 years, inclusive. [+12]

Presence of autoimmune or pathologic causes of hair loss, such as alopecia areat... [+18]

Status: Recruiting

Blood Specimen Collection For Laboratory Assay Research

To collect lab data from capillary and venous blood specimens for use in analytical research studies to support the development and validation of laboratory procedures.

Participants needed: 10,000
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Roman Health Ventures Inc.Updated: Aug 13, 2026Locations: 1
Eligibility criteria

Any gender, in good general health [+5]

Individuals who are unable to provide a blood sample due to any illness [+3]

Status: Not yet recruiting

For an Investigator-led Hair Study Comparing Between Healthy and Hair Loss Volunteers

This study is to evaluate differences in the gut and follicle/scalp microbiome signature in AGA compared to a non-AGA population. Also, to investigate differences in inflammation and other biomarkers in AGA compared to non-AGA population at baseline and after a successful treatment

Participants needed: 66
Trial details
Age: 21-45Biological sex: MaleType: ObservationalSponsor: National Skin CentreUpdated: Jul 21, 2026
Eligibility criteria

Male volunteer from 21 to 45 years old [+10]

Volunteer with severe gastro-intestinal symptoms (including gluten and lactose i... [+33]

Status: Recruiting

Scalp Hair Metabolomics in Severe Obesity

The purpose of this research study is to investigate how body weight and weight-loss surgery affect the natural chemicals found in scalp hair over time. We will also find out how common and severe hair thinning/hair loss and muscle loss are in the first 6 months after bariatric surgery.

Participants needed: 60
Trial details
Age: 21-70Biological sex: AllType: ObservationalSponsor: Singapore General HospitalUpdated: Feb 13, 2026Locations: 1
Eligibility criteria

Age 21-70 years [+6]

Pregnancy [+2]

Status: Recruiting

Clinical Study to Evaluate the Improvement in Hair Loss in Skin of Color Treated With Fractional Non-Ablative Laser

The study incudes 18 to 55 y/o healthy subjects with moderate hair loss stage and Fitzpatrick skin type 5 or 6

Participants needed: 40
Trial details
Age: 21-55Biological sex: AllType: InterventionalSponsor: Lumenis Be Ltd.Updated: Jan 2, 2026Locations: 1
Eligibility criteria

Male and females between 21 - 55 years of age, inclusive. [+14]

Clinical diagnosis of alopecia areata or scarring forms of alopecia [+18]

Status: Recruiting

Study to Assess the Ability of the Portable Scalp Cooling System (PSCS) to Prevent Hair Loss

The purpose of this prospective study is to assess the ability of AMMA to prevent hair loss in women receiving chemotherapy (CT) for early-stage breast cancer. Additionally, the purpose is also to assess the safety, tolerability and compliance, quality of life, and satisfaction with hair preservation after CT treatment.

Participants needed: 99
Trial details
Age: 21+Biological sex: FemaleType: InterventionalSponsor: Cooler Heads Care Inc.Updated: Apr 6, 2025Locations: 2
Eligibility criteria

Female patients ≥ 21 years of age [+8]

Patients with female pattern baldness resembling picture I-3 or higher on the Sa... [+16]

Status: Recruiting

Systemic Treatments for Alopecia Areata Registry

A multicenter prospective registry (STA2R) is conducted to assess systemic treatments for alopecia areata, focusing on effectiveness, safety, and long-term outcomes.

Participants needed: 10,000
Trial details
Age: 16+Biological sex: AllType: ObservationalSponsor: Erasmus Medical CenterUpdated: Feb 28, 2024Locations: 1Duration: 50 Years
Eligibility criteria

Diagnosed with alopecia areata; [+2]

Not sufficiently capable of understanding the Dutch language; [+1]