Overview

Trial on Safety and Pharmacokinetics of Intravaginal Curcumin

Status:
Completed
Trial end date:
2012-01-01
Target enrollment:
Participant gender:
Summary
The main objective of this study is to determine the maximum tolerable dose and safety of intravaginal curcumin in a normal population of women (women with no evidence of cervical cytological abnormalities by pap testing).
Phase:
Phase 1
Details
Lead Sponsor:
Emory University
Treatments:
Curcumin