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Starting soon Observational

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

NCT07869199 · tracked via the Priya Life Science Spain tracker
Phase
Observational
Started
2026-10
Last updated
2026-10-09

Condition(s) studied

Gut DysbiosisTelogen EffluviumHair Loss

Investigational drug(s) / intervention(s)

Drinkable multifactorial food supplement containing vitamins, minerals, plant extracts, and other bioactive compounds, formulated to support hair growth and scalp health in women.

Drinkable multifactorial food supplement containing vitamins, minerals, plant extracts, and other bioactive compounds, formulated to support hair growth and scalp health in women.: Drinkable multifactorial food supplement in liquid form, administered once daily in a 25 mL single-dose vial, for a duration of 180 days. The formulation contains a combination of vitamins, minerals, plant extracts, amino acids, and other bioactive compounds designed to support hair growth and scalp health in women.

Study summary

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.

Eligibility

Sex
FEMALE
Min age
18 Years
Max age
40 Years
Healthy volunteers
No
Inclusion Criteria: * Women aged 18-40 years. * Premenopausal status. * Diagnosis of telogen effluvium (TE) lasting more than 3 months. * Digestive symptoms with no diagnosed underlying disease (gut microbiota dysbiosis). Exclusion Criteria: * Moderate or severe irritable bowel syndrome (IBS). * Small intestinal bacterial overgrowth (SIBO). * Prior use of the study product. * Participation in similar studies or use of anti-hair-loss products within the previous 3 months. * Skin or scalp diseases or disorders (e.g., psoriasis, dermatitis, eczema, cicatricial alopecia, or alopecia areata). * Alopecia secondary to any medical condition (e.g., hypothyroidism, anaemia, lupus). * Chronic pharmacological treatment or a diagnosed systemic disease. * Pregnancy, postpartum period (within 6 months), or breastfeeding. * Previous abdominal surgery (except hysterectomy and appendectomy). * Perimenopausal or menopausal status.

Primary outcome measure(s)

  • Characterization of gut dysbiosis outcomes — 6 months
    Gus dysbiosis was analyzed with a stool kit test (KyberBioma(R)).
  • Characterization of trichoscopic outcomes — 6 months
    Trychoscopy outcomes were measured using a phototrichoscope at the interparietal area. 7 trichoscopy signs were graded (0-3) from 2 evaluators: telangiectasias, punctate vessels, erythema, scaling, follicular miniaturization, follicular hyperkeratosis, fibrosis.

Trial sites (2)

FacilityCityRegionStatus
Clínica AB Derma Madrid Madrid
Clínica Hbn39 Madrid Madrid
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07869199 on ClinicalTrials.gov ↗ ← All trials in Spain