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Epidermal Cell Transplantation in Vitiligo Skin (VITICELL)

Primary Purpose

VITILIGO

Status
Completed
Phase
Phase 2
Locations
France
Study Type
Interventional
Intervention
Grafting with epidermal cells
UVB treatment
Sponsored by
Centre Hospitalier Universitaire de Nice
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for VITILIGO

Eligibility Criteria

18 Years - 85 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Age > 18yr
  • Stable vitiligo (no lesion since 12 mo)
  • 2 symmetrical vitiligo patches of at least 10 cm2
  • Vitiligo requiring UVB treatment
  • Women using a contraceptive

Exclusion Criteria:

  • History of keloids
  • History of skin cancer
  • Photosensitivity
  • Positive blood test for HIV, HBV, HVC, or HTLV1
  • Pregnant or breastfeeding women

Sites / Locations

  • Centre hospitalier Universitaire de Nice

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

A: Grafting of autologous epidermal harvested cells and UVB

UVB treatment

Arm Description

Grafting with epidermal cells: A superficial skin shaving excision will be obtained from pigmented skin using a dermatome. A cell suspension will be obtained by trypsinisation. Vitiligo skin will be dermabraded by Erbium: Yag laser after local anaesthesia. The cell suspension will be spread on the dermabraded skin area and fixed with dressings. Keratinocyte, and melanocyte counts will be performed on an aliquot of the cell suspension. One symmetrical patch of vitiligo will be chosen as control and left untreated. Narrow-band UVB treatment: Four weeks after transplantation of epidermal cells, the grafted and control patch will be treated by Narrow-band UVB. Treatment will be performed 2 times a week. Narrow-band UVB treatment will be performed for at least 3 months or 24 treatments.

UVB treatment twice a week during 3months

Outcomes

Primary Outcome Measures

Repigmentation rate at 12 months
Repigmentation rate at 12 months

Secondary Outcome Measures

Repigmentation > 70% at 12 months
Repigmentation > 70% at 12 months

Full Information

First Posted
March 23, 2012
Last Updated
May 29, 2013
Sponsor
Centre Hospitalier Universitaire de Nice
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1. Study Identification

Unique Protocol Identification Number
NCT01629979
Brief Title
Epidermal Cell Transplantation in Vitiligo Skin
Acronym
VITICELL
Official Title
Efficacy and Tolerance of Transplantation of Harvested Epidermal Cells and Narrow-Band UVB in Vitiligo
Study Type
Interventional

2. Study Status

Record Verification Date
May 2013
Overall Recruitment Status
Completed
Study Start Date
May 2011 (undefined)
Primary Completion Date
November 2012 (Actual)
Study Completion Date
November 2012 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Centre Hospitalier Universitaire de Nice

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The effects of treatment of transplantation of harvested autologous epidermal cells on vitiligo lesions followed by narrow-band UVB will be investigated in a randomized controlled study.
Detailed Description
Introduction: Transplantation of harvested autologous epidermal cells in vitiligo is widely used in vitiligo but randomized controlled trials in the literature investigating the efficacy of these noncultured keratinocyte/melanocyte suspensions are scarce. In addition there are few data regarding the relationship between the cellular contents of epidermal suspensions and the clinical outcome. Aim of the study: To perform a prospective, controlled, randomized, intra-individual comparative study in vitiligo lesions treated with epidermal cell transplantation with additional narrow-band UVB treatment using epidermal cell suspensions that have been characterized at the cellular level. Study design: Grafting with epidermal cells: A superficial skin shaving excision will be obtained from pigmented skin using a dermatome. A cell suspension will be obtained by trypsinisation. Vitiligo skin will be dermabraded by Erbium: Yag laser after local anaesthesia. The cell suspension will be spread on the dermabraded skin area and fixed with dressings. Keratinocyte, and melanocyte counts will be performed on an aliquot of the cell suspension. One symmetrical patch of vitiligo will be chosen as control and left untreated. Narrow-band UVB treatment: Four weeks after transplantation of epidermal cells, the grafted and control patch will be treated by Narrow-band UVB. Treatment will be performed 2 times a week. Narrow-band UVB treatment will be performed for at least 3 months or 24 treatments. Evaluation of the treatment success: The grade of pigmentation in all lesions will be evaluated clinically, with photographs. The clinical rating will be performed as follows: 0 = no repigmentation; 1 = 1-25% repigmentation; 2 = 26 to 50% repigmentation; 3 = 51 to 75% repigmentation; and 4 = 76 to 100% repigmentation. The evaluation of the photographs will be performed blinded by physicians not engaged in the treatment phase of the study. In addition the surface of vitiligo patches will be traced on transparent sheets and monitored by planimetry.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
VITILIGO

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2, Phase 3
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
23 (Actual)

8. Arms, Groups, and Interventions

Arm Title
A: Grafting of autologous epidermal harvested cells and UVB
Arm Type
Experimental
Arm Description
Grafting with epidermal cells: A superficial skin shaving excision will be obtained from pigmented skin using a dermatome. A cell suspension will be obtained by trypsinisation. Vitiligo skin will be dermabraded by Erbium: Yag laser after local anaesthesia. The cell suspension will be spread on the dermabraded skin area and fixed with dressings. Keratinocyte, and melanocyte counts will be performed on an aliquot of the cell suspension. One symmetrical patch of vitiligo will be chosen as control and left untreated. Narrow-band UVB treatment: Four weeks after transplantation of epidermal cells, the grafted and control patch will be treated by Narrow-band UVB. Treatment will be performed 2 times a week. Narrow-band UVB treatment will be performed for at least 3 months or 24 treatments.
Arm Title
UVB treatment
Arm Type
Active Comparator
Arm Description
UVB treatment twice a week during 3months
Intervention Type
Procedure
Intervention Name(s)
Grafting with epidermal cells
Intervention Description
A superficial skin shaving excision will be obtained from pigmented skin using a dermatome. A cell suspension will be obtained by trypsinisation. Vitiligo skin will be dermabraded by Erbium: Yag laser after local anaesthesia. The cell suspension will be spread on the dermabraded skin area and fixed with dressings. Keratinocyte, and melanocyte counts will be performed on an aliquot of the cell suspension. One symmetrical patch of vitiligo will be chosen as control and left untreated. Narrow-band UVB treatment: Four weeks after transplantation of epidermal cells, the grafted and control patch will be treated by Narrow-band UVB. Treatment will be performed 2 times a week. Narrow-band UVB treatment will be performed for at least 3 months or 24 treatments.
Intervention Type
Radiation
Intervention Name(s)
UVB treatment
Intervention Description
the control patch will be treated by Narrow-band UVB. Treatment will be performed 2 times a week. Narrow-band UVB treatment will be performed for at least 3 months or 24 treatments.
Primary Outcome Measure Information:
Title
Repigmentation rate at 12 months
Description
Repigmentation rate at 12 months
Time Frame
12months
Secondary Outcome Measure Information:
Title
Repigmentation > 70% at 12 months
Description
Repigmentation > 70% at 12 months
Time Frame
12 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
85 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age > 18yr Stable vitiligo (no lesion since 12 mo) 2 symmetrical vitiligo patches of at least 10 cm2 Vitiligo requiring UVB treatment Women using a contraceptive Exclusion Criteria: History of keloids History of skin cancer Photosensitivity Positive blood test for HIV, HBV, HVC, or HTLV1 Pregnant or breastfeeding women
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
philippe bahadoran, doctor
Organizational Affiliation
Centre Hospitalier Universitaire de Nice
Official's Role
Principal Investigator
Facility Information:
Facility Name
Centre hospitalier Universitaire de Nice
City
Nice
ZIP/Postal Code
06000
Country
France

12. IPD Sharing Statement

Learn more about this trial

Epidermal Cell Transplantation in Vitiligo Skin

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