Autologous Cell Suspension Grafting Using ReCell in Vitiligo and Piebaldism Patients
Launched by NETHERLANDS INSTITUTE FOR PIGMENT DISORDERS · May 27, 2015
Trial Information
Current as of August 11, 2025
Completed
Keywords
ClinConnect Summary
Autologous epidermal cell suspension grafting is an effective method of surgical treatment in vitiligo, which is suitable for treating large areas with good cosmetic results. The ReCell Autologous Cell Harvesting Device (Avita Medical Europe Limited, Cambridge, UK) is a device which, compared to other forms of autologous epidermal cell suspension grafting, is easier in use showing similar results. With this device an epidermal cell suspension is created from a split skin graft, usually taken from the hip region. Currently, conventional ablative (full surface de-epidermisation) laser treatme...
Gender
ALL
Eligibility criteria
- Inclusion Criteria:
- • Patients with, segmental vitiligo or piebaldism under medical treatment at the Netherlands Institute for Pigment Disorders
- • Age ≥18
- • Patient is willing and able to give written informed consent
- • Segmental vitiligo stable since 12 months without systemic therapy or 12 months without topical therapy as defined by the absence of new lesions and/or enlargement of existing lesions.
- • At least four depigmented lesions on the proximal extremities or trunk larger than 3x3 cm or one depigmented lesion on the proximal extremities or trunk of at least 12x3 cm.
- Exclusion Criteria:
- • UV therapy or systemic immunosuppressive treatment during the last 12 months
- • Local treatment of vitiligo during the last 12 months
- • Vitiligo lesions with follicular or non-follicular repigmentations
- • Skin type I
- • Recurrent HSV skin infections
- • Hypertrophic scars
- • Keloid
- • Cardiac insufficiency
- • Patients with a history of hypersensitivity to (UVB or UVA) light and/or allergy to local anaesthesia.
- • Patients who are pregnant or breast-feeding
- • Patients not competent to understand what the procedures involves
- • Patients with a personal history of melanoma or non-melanoma skin cancer
- • Patients with atypical nevi.
- • Known allergy to clarithromycin
About Netherlands Institute For Pigment Disorders
The Netherlands Institute for Pigment Disorders is a leading research organization dedicated to advancing the understanding and treatment of pigment-related conditions. Focusing on innovative clinical trials, the institute aims to develop effective therapeutic strategies for disorders such as vitiligo, melasma, and other pigmentary anomalies. With a multidisciplinary team of experts, the institute fosters a collaborative environment that integrates cutting-edge research with clinical practice, ensuring that patients benefit from the latest advancements in dermatological science. Committed to improving patient outcomes, the institute prioritizes safety, efficacy, and ethical standards in all its clinical studies.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Amsterdam, , Netherlands
Patients applied
Trial Officials
Albert Wolkerstorfer, MD, PhD
Principal Investigator
Netherlands Institute for Pigment Disorders, Department of Dermatology, Academic Medical Center, University of Amsterdam
Menno A. De Rie, MD, PhD
Study Director
Department of Dermatology, Academic Medical Center, University of Amsterdam
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported
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