Hi all, we are looking for healthy volunteers willing to participate in a clinical study involving a rare disease called Epidermolysis Bullosa Simplex (EBS). Currently, there is no treatment for EBS, and our goal for this study is to identify new drugs that might help EBS patients with wound healing and pain reduction. Your participation in this study is completely voluntary. The procedures will occur all in one day, and as a participant you will have the following performed: a small punch biopsy of your skin and a blood draw. This study will compare gene expression differences between skin from individuals with EBS as well as normal skin from healthy individuals. Your participation in the study will be as a healthy control.
Please call or message us if you are interested!
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STANFORD DERMATOLOGY
ELIGIBILITY:
1. Male or Female
2. Age: 20 years or older
3. No diagnosis of EBS
WHAT:
1. 1 skin punch biopsy
2. 1 blood draw
3. 1 visit of approximately 30 minutes and no other visits or testing
Compensation: $50 after completion of study
INTERESTED? Contact Us:
To find out if you are eligible and for further information concerning this study, please contact the study coordinator at
pediatricdermstudy@stanford.edu.
Participant's rights questions, contact 1-866-680-2906.
Please feel free to email us for additional information. Thank you for your interest in helping families with this rare condition.
Please call or message us if you are interested!
-----------------------------------------
STANFORD DERMATOLOGY
ELIGIBILITY:
1. Male or Female
2. Age: 20 years or older
3. No diagnosis of EBS
WHAT:
1. 1 skin punch biopsy
2. 1 blood draw
3. 1 visit of approximately 30 minutes and no other visits or testing
Compensation: $50 after completion of study
INTERESTED? Contact Us:
To find out if you are eligible and for further information concerning this study, please contact the study coordinator at
pediatricdermstudy@stanford.edu.
Participant's rights questions, contact 1-866-680-2906.
Please feel free to email us for additional information. Thank you for your interest in helping families with this rare condition.
