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NCT Number: NCT07705217

The Role of Gut and Skin Microbiota in Alopecia Areata

The goal of this clinical trial is to learn if fecal microbiota transplantation (FMT) works to treat alopecia areata in adults. It will also learn about the safety of FMT. The main questions it aims to answer are:

* Can FMT cause hair regrowth? * Can FMT modulate immune response? Researchers will compare FMT to a placebo (a look-alike substance that contains no drug) to see if FMT works to treat alopecia areata.

Participants will:

* Take FMT or a placebo for three consecutive days * Follow-up evaluations will be performed at weeks 12, 24, and 48, with repeat clinical scoring, photodocumentation, microbiome analyses, laboratory testing, and quality-of-life assessment.

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Key information

Age range

18 year–65 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Polyclinic GrandMed

Opatija, Croatia

Location contact

Tea Rosovic, Dermatovenerology specialist

CONTACT

[email protected]

+00385913737237

Tea Rosovic, Dermatovenerology specialist

PRINCIPAL_INVESTIGATOR

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Adults aged 18-65 diagnosed with Alopecia Areata (patchy or extensive) up to 10 years
  • Willingness to adhere to study protocols, including FMT administration via capsules or colonoscopy.
  • Ability to sign informed consent.
  • SALT score≥ 20

Exclusion criteria

  • History of gastrointestinal disorders (e.g., IBD, celiac disease).
  • Recent use of antibiotics, probiotics, or prebiotics (within 2 months).
  • Pregnant or breastfeeding women of childbearing potential who are unwilling or unable to use an acceptable method of birth control.
  • Individuals with immunocompromised or immunosuppressed states (e.g., HIV, cancer).
  • Prior FMT treatment for any condition.
  • Therapy with new antidepressants or had a change in antidepressant dose within previous 3 months
  • Serious medical comorbidities(including neurological or phychiatric comorbidities)
  • Elevated C-reactive protein concentration, abnormal baseline laboratory tests
  • Severe(anaphylactic) food allergy
  • Concomitant treatments for AA: topical KS 1 week prior to randomization, topical JAK inhibitor, diphenylcyclopropenone, or other topical immunotherapies within 4 weeks prior to randomization;systemic corticosterids, immunosuppressant, intra-lesional or intra-articular corticosteroid injections, or oral JAK inhibitor within 8 weeks prior to randomization;monoclonal antibody <5 half-lives prior to randomization; probenecid at the time of randomization. Bimatoprost ophtalmic solution was allowed if on stable dose for 8 weeks.

Treatment and study plan

Fecal Microbial Transplant Enema

Other

Patients with alopecia areata will recieve FMT or in the 3 capsules for three consecutive days or FMT via colonoscopy

Other names: FMT

Placebo

Other

Patients will recieve three capsules with inert material or saline via colonoscopy

Primary outcomes

  1. Changes in hair growth- Severity of Alopecia Tool

    Time frame: From enrollment to the end of treatment at 48 weeks

    The primary success will be a statistically significant difference in hair regrowth between the Fecal Microbiota transplantation (FMT) group and placebo group at weeks 24 and 48, assessed as a binary endpoint (regrowth yes/no) and supported by changes in SALT (Severity of Alopecia Tool) score as a standardized measurement used to quantify scalp hair loss in patients with alopecia areata. The scale ranges from 0 (no hair loss) to 100 (complete scalp hair loss). A clinically meaningful reduction in SALT score (≥50% improvement from baseline) will be considered a strong indicator of therapeutic efficacy.

  2. Changes in hair growth- Alopecia Areata Investigator Global Assessment

    Time frame: From enrollment to the end of treatment at 48 weeks

    The primary success will be a statistically significant difference in hair regrowth between the Fecal Microbiota transplantation (FMT) group and placebo group at weeks 24 and 48, assessed as a binary endpoint (regrowth yes/no) and supported by changes in Alopecia Areata Investigator Global Assessment (AA-IGA) to measure five clinically meaningful gradations of alopecia areata scalp-hair loss that reflects patients' and clinicians' perspectives and expectations of treatment success in alopecia areata treatment studies. The AA-IGA score is based on the patient's SALT score. The scale is numbered from 0, which corresponds to 0% of hair loss (ie, SALT 0), indicating no hair loss, to 4, which corresponds to 95-100% of hair loss (ie, SALT 95-100), indicating very severe hair loss.

  3. Changes in hair growth- The Alopecia Areata Scale

    Time frame: From enrollment to the end of treatment at 48 weeks

    The primary success will be a statistically significant difference in hair regrowth between the Fecal Microbiota transplantation (FMT) group and placebo group at weeks 24 and 48, assessed as a binary endpoint (regrowth yes/no) and supported by changes in The Alopecia Areata Scale (AASc) in wich primary criterion is Severity of scalp hair loss: mild 20% or less, moderate 21-49%, severe 50-100% scalp hair loss. Secondary criteria: is any is present, increase severity rating by one level: noticeable involvement of eyebrows or eyelashes; inadequate response after at least 6 months of treatment; negative impact on psychosocial functioning resulting from AA; diffuse (multifocal) positive hait pull test consistent with pidly progressive alopecia areata.

  4. Fecal microbiota transplantation modulation of the gut and skin microbiota

    Time frame: From enrollment to the end of treatment at 48 weeks

    The primary objective of this proposal is to test the hypothesis that fecal microbiota transplantation (FMT) induces beneficial modulation of the gut and skin microbiota, leading to immunoregulatory effects in patients with alopecia areata (AA). Characterize baseline skin, and colonic mucosal microbiota composition in patients with AA using 16S rRNA sequencing of skin and colon musosa biopsy specimens and assess changes following FMT.

  5. Change in T cell subsets from Baseline to 48 weeks

    Time frame: From enrollment to the end of treatment at 48 weeks

    Before and after Fecal microbiota transplantation patient will be taken 60-80 ml of peripheral blood for:

    • CBC, CRP
    • Flow cytometry analyses: Tumor necrosis factor alfa (TNFɑ), IL-10, IL-18, IFN-γ, IL-15, IL-2 and trichohyalin; CD4+ Th1 lymphocytes, CD8+ cytotoxic T cells, IFN-γ-producing lymphocytes, CXCR3+ T cells, NK cells, ILC1-like innate lymphoid cells, activated T cells expressing CD69 and HLA-DR, and regulatory T cells (CD4+CD25+FOXP3+)

Study contacts

Contact information is provided by the study sponsor or research team.

Tea Rosovic, Dermatovenerology specialist

CONTACT

[email protected]

+00385913737237

Sponsors and collaborators

Lead sponsor

Polyclinic GrandMed

Other

Registry information

Acronym: RGSM-AA-ICS

Important dates

Study start
2026
Primary completion
2027
Study completion
2027
First posted
Jul 15, 2026
Registry last updated
Jul 15, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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