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Trial on Safety and Pharmacokinetics of Intravaginal Curcumin

Uterine Cervical Dysplasia Clinical Trial

Official title:
Phase I Trial on Safety and Pharmacokinetics of Intravaginal Curcumin in Normal Female Subjects

Clinical Trial 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).

Clinical Trial Description

n/a

Study Design

Endpoint Classification: Safety Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT01035580
Study type Interventional
Source Emory University
Contact
Status Completed
Phase Phase 1
Start date January 2010
Completion date January 2012
View Details
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