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Spots Global Cancer Trial Database for Phase 3 Study of Imiquimod Creams in the Treatment of External Genital Warts

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Trial Identification

Brief Title: Phase 3 Study of Imiquimod Creams in the Treatment of External Genital Warts

Official Title: A Safety and Effectiveness Study of Imiquimod Creams in the Treatment of External Genital Warts

Study ID: NCT00735462

Conditions

Genital Warts

Study Description

Brief Summary: The purpose of this study is to determine whether imiquimod creams are effective in treating external genital warts (EGW). The secondary objective of this study is to provide information on recurrence of EGW. Additionally the study will also look at any adverse events associated with the use of the creams. External genital and perianal warts are caused by the infection of human papillomavirus or HPV. HPV infection is a sexually transmitted disease (STD). External genital warts look like small flesh-colored, pink, or red growths on or around the external skin of sex organs or perianal area. The warts may look similar to the small parts of a cauliflower or they may be very tiny and difficult to see. They often appear in clusters of three or four, and may grow and spread rapidly. They usually are not painful, although they may cause mild pain, bleeding, and itching.

Detailed Description:

Eligibility

Minimum Age: 12 Years

Eligible Ages: CHILD, ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

NEA Clinic, Jonesboro, Arkansas, United States

Northern Claifornia Research, Carmichael, California, United States

California State University - Chico, Chico, California, United States

Dermatology Research Associates, Los Angeles, California, United States

Conant Foundation, San Francisco, California, United States

Downtown Women's Healthcare, Denver, Colorado, United States

Altus Research, Lake Worth, Florida, United States

PMI Health Research Group, Atlanta, Georgia, United States

Atlanta Women's Research Institute, Atlanta, Georgia, United States

Altman Dermatology Associates, Arlington Heights, Illinois, United States

Howard Brown, Chicago, Illinois, United States

Valley Medical Center, Flint, Michigan, United States

Women's OB/GYN, Saginaw, Michigan, United States

Clayton Research Institute, St Louis, Missouri, United States

Alliance Women's Research, Delran, New Jersey, United States

Women's Health Research Center, Lawrenceville, New Jersey, United States

Southwest Clinical Research, Albuquerque, New Mexico, United States

University Urology Associates, New York, New York, United States

Boro Park ObGyn, New York, New York, United States

Crescent Medical Research, Salisbury, North Carolina, United States

Piedmont Medical Research, Winston-Salem, North Carolina, United States

Rapid Medical Research, Cleveland, Ohio, United States

Complete Healthcare for Women, Columbus, Ohio, United States

Wright State University, Dayton, Ohio, United States

Heartland Health Institute, Tulsa, Oklahoma, United States

Clinical Trials of America, Eugene, Oregon, United States

Westover Heights Clinic, Portland, Oregon, United States

The Clinical Trial Center, Jenkintown, Pennsylvania, United States

Palmetto Clinical Research, Greer, South Carolina, United States

Alpha Clinical Research, Clarksville, Tennessee, United States

Adams Patterson Gynecology and Obstetrics, Memphis, Tennessee, United States

Tennessee Women's Care, Nashville, Tennessee, United States

DiscoveResearch, Bryan, Texas, United States

TMC Life Research, Houston, Texas, United States

West Houston Clinical Research Services, Houston, Texas, United States

Urology San Antonio Research, San Antonio, Texas, United States

The Center for Clinical Studies, Webster, Texas, United States

Utah Clinical Trials, Salt Lake City, Utah, United States

Wasatch Clinical Research, Salt Lake City, Utah, United States

CARE-ID, Annandale, Virginia, United States

Tidewater Clinical Reseach, Virginia Beach, Virginia, United States

Independence Family Medicine Clinical Research, Virginia Beach, Virginia, United States

Women's Clinical Research Center, Seattle, Washington, United States

Contact Details

Name: Jason Wu, MD

Affiliation: Graceway Pharmaceuticals

Role: STUDY_DIRECTOR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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