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An exploratory clinical trial for the congenital melanocytic nevi using the combination therapy with the inactivated autologous nevus tissue by high hydrostatic pressure and the cultured epithelial autograft

Phase 1
Conditions
Congenital melanocytic nevi
Registration Number
JPRN-UMIN000030771
Lead Sponsor
Department of Plastic and Reconstructive Surgery, Kansai Medical University
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete: follow-up complete
Sex
All
Target Recruitment
3
Inclusion Criteria

Not provided

Exclusion Criteria

1.Patients with scar tissue that prevent the take of inactivated nevus 2.The nevus that has been treated by cultured epidermal autografts in previous clinical trials

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
The epithelialization grafted site at 12 weeks after the implantation
Secondary Outcome Measures
NameTimeMethod
The operability assessment of high hydrostatic pressurization of nevus tissue
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