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Clinical Trial Details — Status: Withdrawn

Administrative data

NCT number NCT00382330
Other study ID # 0120050348
Secondary ID
Status Withdrawn
Phase N/A
First received September 27, 2006
Last updated September 5, 2013

Study information

Verified date April 2013
Source Rutgers, The State University of New Jersey
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Interventional

Clinical Trial Summary

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.


Recruitment information / eligibility

Status Withdrawn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.

Study Design

Allocation: Non-Randomized, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Prevention


Related Conditions & MeSH terms


Intervention

Drug:
Ciclopirox


Locations

Country Name City State
United States University of Medicine and Dentistry of NJ Newark New Jersey

Sponsors (1)

Lead Sponsor Collaborator
University of Medicine and Dentistry of New Jersey

Country where clinical trial is conducted

United States, 

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