Clinical Trials Directory

Trials / Completed

CompletedNCT02156427

Evaluation of Non-cultured Epidermal Cellular Grafting vs Hyaluronic Acid for Repigmenting Vitiligo and Piebaldism

A Multicenter Double-blind Placebo-controlled Trial of Non-cultured Epidermal Cellular Grafting Versus Hyaluronic Acid for Repigmenting Stable Leukoderma (Vitiligo and Piebaldism)

Status
Completed
Phase
Phase 3
Study type
Interventional
Enrollment
38 (actual)
Sponsor
Laboratoires Genévrier · Industry
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to assess the efficacy of autologous epidermal cells suspension grafting using a newly developed device named VITICELL® compared to placebo. The secondary objective is to evaluate safety of VITICELL® and global satisfaction of patient and investigator.

Conditions

Interventions

TypeNameDescription
DEVICEVITICELLgraft of autologus cells (kaeratonicytes and melanocytes) obtained after trypsinization of thin skin biopsy resuspended into hyaluronic acid
DEVICEPLACEBOhyaluronic acid alone

Timeline

Start date
2014-04-29
Primary completion
2018-04-10
Completion
2018-04-10
First posted
2014-06-05
Last updated
2019-10-14

Locations

5 sites across 3 countries: Belgium, France, Italy

Source: ClinicalTrials.gov record NCT02156427. Inclusion in this directory is not an endorsement.

Evaluation of Non-cultured Epidermal Cellular Grafting vs Hyaluronic Acid for Repigmenting Vitiligo and Piebaldism (NCT02156427) · Clinical Trials Directory