Use of Epidermal Expansion System for Epidermal Grafting on Hypopigmented Skin and Surgical Wounds
Status unconfirmed · Not applicable
Conditions studied: Surgical Wound, Hypo-pigmented Skin
In brief
This case series will assess the use of suction blister epidermal grafts harvested by a novel device on select patients with hypo pigmented skin or surgical skin wounds.
Key facts
- Study ID
- NCT01590329
- Run by
- Momelan Technologies
- People needed
- 12
- Starts
- 2012-03-01
- Expected to finish
- 2012-10-01
- Last updated by the study team
- 2012-05-02
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Male or female adult subject between 18 and 99 years of age
- Subject having an area of hypopigmentation or surgical wound considered appropriate by physician to receive epidermal micro grafting
- Willingness to participate in study by evidence of informed consent
You may not qualify if…
- Female subjects self-reported to be breastfeeding, pregnant or planning to become pregnant during the course of the study.
- Subject showing clinical signs of infection
- Subjects currently on immunosuppressive medications, chemotherapy or cytotoxic agents
- Subject participation in another interventional study with potential exposure to an investigational drug or device within the past 30 days or planned entry into another investigational study within 90 days after entrance into this study
Where it is running
- Laser and Skin Surgery Center of New York — New York, New York, United States (enrolling)
Full record on ClinicalTrials.gov
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