Active, not recruitingPHASE1, PHASE2NCT04967170
A Study to Evaluate Platelet Rich Plasma to Treat Vulvar Lichen Sclerosus
Studying Rapidly involuting congenital hemangioma
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- Jennifer R. Arthurs
- Principal Investigator
- Katherine Bodiford, MDMayo Clinic
- Intervention
- Autologous Platelet-Rich Plasma (PRP)(biological)
- Enrollment
- 30 target
- Eligibility
- 18 years · FEMALE
- Timeline
- 2022 – 2026
Study locations (1)
- Mayo Clinic in Florida, Jacksonville, Florida, United States
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
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