Cytokine Profiling in Vulvovaginal Lichen Planus
Why is this study being done?
The purpose of this study is to figure out how cell signaling molecules called cytokines change during a flare of VVLP.
Participation in this study involves two in-person visits; one when you are having VVLP symptoms and one when you are not having VVLP symptoms. The first visit will include the consent process and will last an hour, while the second visit will last under 30 minutes. Each visit will include one blood draw and optional clinical photos to standardize the description of VVLP among doctors. You will also be asked to complete three surveys about your symptoms and quality of life.
Eligibility
You may be eligible to participate in this study if you:
- Are between the ages 18 and 85
- Have a diagnosis of vulvovaginal lichen planus, also called VVLP
- Are willing to attend 2 study visits – one when you are having symptoms and one when you are not having symptoms\Are not currently using systemic treatment (topical treatments are OK)
Compensation
You will be compensated $25 for each blood draw you complete. If you allow photographs to be taken at both visits, you will be compensated an additional $25. Maximum compensation is $75.
Contact Information
To find out more information and to learn if you are qualified to participate, fill out the online form.
or call the Women’s Health Research Unit confidential recruitment line at 503-494-3666 or email us at whru@ohsu.edu.
Contact us
To find out more information and to learn if you are qualified to participate, fill out the online form or call the Women’s Health Research Unit confidential recruitment line at 503-494-3666 or email us at whru@ohsu.edu.
About the study
- Principal Investigator: Erin Foster, M.D., Ph.D.
- IRB #29996