Autologous Non-cultured Epidermal Cell Suspension Transplantation in the Treatment of Vitiligo

ConditionVitiligo
Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age8-65
SponsorPeking University People's Hospital

About this trial

To observe the long-term efficacy and safety of autologous non cultured epidermal cell suspension transplantation in the treatment of vitiligo, analyze the correlation between cell density, type, and postoperative efficacy and prognosis, and providing a basis for clinical application.

Eligibility criteria

Qualifiers

Patients diagnosed as vitiligo, according to the "Vitiligo Diagnosis and Treatment Consensus (2021 edition)

Segmental and unclassified vitiligo stable for 6 months, Non-segmental vitiligo stable for 1 year and resistant to medication and phototherapy

BSA≥5%

Sign the informed consent and be willing to undergo surgical treatment

Disqualifiers

Severe visceral or infectious disease not suitable for surgical treatment

Tendency toward keloid formation

Coagulation defects

Unable to complete follow-up on time

Trial design

Treatments tested in this trial

  • Autologous Non-cultured Epidermal Cell Suspension transplantation

Treatment groups

30 Participants
are divided into 1 treatment group