Vulvar Cancer Clinical Trial
Official title:
Chemoprevention of Cancer in the Lower Female Genital Tract: The Antineoplastic Activity of the Fungicide Ciclopirox.
NCT number | NCT00382330 |
Other study ID # | 0120050348 |
Secondary ID | |
Status | Withdrawn |
Phase | N/A |
First received | September 27, 2006 |
Last updated | September 5, 2013 |
The purpose of this study is to determine if regular and daily repeated application of the ciclopirox lotion to vulva will make the precancerous lesion(s) shrink or even disappear.
Status | Withdrawn |
Enrollment | 0 |
Est. completion date | |
Est. primary completion date | |
Accepts healthy volunteers | |
Gender | Female |
Age group | 18 Years to 75 Years |
Eligibility |
Inclusion Criteria: - Patients between the ages 18 and 75 years. - Patients may be carriers of the Human Immunodeficiency Virus (HIV). - Patients must have been diagnosed with precancerous lesion(s) of the vulva by tissue sampling (biopsy-proven vulvar intraepithelial neoplasia grade II or III) - Patients must be able to come to University Hospital for their initial appointment in Gynecologic Oncology Clinic, and for the eight follow-up visits in that Clinic required by the protocol. Exclusion Criteria: - Pregnant or patients who are breast feeding a baby. - Patients who have been diagnosed with a vaginal yeast infection. - Patients who have undergone prior surgery for precancerous lesion(s) of the vulva. |
Allocation: Non-Randomized, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Prevention
Country | Name | City | State |
---|---|---|---|
United States | University of Medicine and Dentistry of NJ | Newark | New Jersey |
Lead Sponsor | Collaborator |
---|---|
University of Medicine and Dentistry of New Jersey |
United States,
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