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Autologous-cultured epithelium sheet for vitiligo vulgaris

Clinical research for autologous-cultured epithelium sheet transplantation for vitiligo vulgaris - Autologous-cultured epithelium sheet for vitiligo vulgaris

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
JPRN
Registry ID
JPRN-jRCTb030200129
Enrollment
5
Registered
2020-09-24
Start date
2022-10-12
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Vitiligo vulgaris

Interventions

Transplantation of processed (autologous-cultured epithelium sheet) cells

Sponsors

Nishikawa Ayaka
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: (1)Patients who are over 20 years old and obtain consent in writing. (2) Patients with a diagnosis of vitiligo vulgaris who have little or no effect on at least a few standard treatments (3) Patients with stable vitiligo that has not progressed within the past year and does not show obvious Koebner phenomenon

Exclusion criteria

Exclusion criteria: (1) Patients being treated for autoimmune diseases (2) Patients who are systemically administered steroids (corticosteroids) (3) Patients with skin malignancy, patients with suspected skin malignancy, or patients with a history of skin malignancy less than 5 years (4) Pregnant women, lactating women, patients who may be pregnant, patients who wish to become pregnant during the study period (5) Patients with severe heart disease (6) Patients with severe liver disease (7) End stage renal failure (8) Patients with severe blood coagulation disorder (9) Person with active infection (10) Persons with mental illness (11) HCV antibody, HBs antigen, HTLV-1 virus antibody or HIV antibody positive (12) Patients with allergic symptoms in cattle and mice (13)Patients with vitiligo area that cannot be covered with Specific Cell Products to be transplanted (14)Other patients who are determined to be inappropriate for participation in this study by the person in charge

Design outcomes

Primary

MeasureTime frame
Number of occurrences of serious adverse events

Secondary

MeasureTime frame
Evaluate below contents, Successive observation of transplantation site Healing satisfaction survey Pain Transplant site infection

Countries

Japan

Contacts

Public ContactDaisuke Mimura

Shonan Beauty Clinic, Shinjuku

mimura@sbc.or.jp+81-50-5865-5944

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026