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Clinical Trials in China / NCT07187882
Recruiting Not applicable

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

NCT07187882 · tracked via the Priya Life Science China tracker
Sponsor
Peking University People's Hospital
Phase
Not applicable
Started
2024-04-25
Last updated
2025-09-23

Condition(s) studied

Vitiligo

Investigational drug(s) / intervention(s)

Autologous Non-cultured Epidermal Cell Suspension transplantation

Autologous Non-cultured Epidermal Cell Suspension transplantation: 1. Thin split thickness skin grafts were taken from the donor site (anterolateral thigh) after application of topical anaesthesia under complete aseptic precautions. 2. The cell suspension was prepared by the cell sorting kit (Primcell, Jiangsu Repatec Life Science Co.,Ltd). 3. Then the recipient skin was uniformly dermabraded using an electrical dermabrader set at 10,000 to 20,000 rpm until punctate bleeding points appeared. 4. The cell suspension was applied onto the dermabraded recipient area. 5. The recipient site was then fixed firmly with dressings and elastic bandage. The dressings were removed 10 days after transplantation.

Study summary

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

Sex
ALL
Min age
8 Years
Max age
65 Years
Healthy volunteers
No
Inclusion Criteria: * 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 * 8-65 years old, both genders Exclusion Criteria: * Severe visceral or infectious disease not suitable for surgical treatment * Tendency toward keloid formation * Coagulation defects * Unable to complete follow-up on time

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Peking University People's Hospital Beijing Beijing Municipality Recruiting

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Other trials for the same condition

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 NCT07187882 on ClinicalTrials.gov ↗ ← All trials in China