Spots Global Cancer Trial Database for Longitudinal Clinical Evaluation of the HPV Assay on the BD VIPER LT System With Cervical Specimens
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Trial Identification
Brief Title: Longitudinal Clinical Evaluation of the HPV Assay on the BD VIPER LT System With Cervical Specimens
Official Title: Longitudinal Clinical Evaluation of the HPV Assay on the BD VIPER LT System With Cervical Specimens
Study ID: NCT02267876
Study Description
Brief Summary: The purpose of the study is to assess the cumulative disease detection of greater than or equal to Cervical intraepithelial neoplasia 2 (CIN2) and greater than or equal to Cervical intraepithelial neoplasia 3 (CIN3) in the subjects over 3 years using the subject's HPV status and cytology status from the BDS-USHPV baseline results
Detailed Description:
Keywords
Eligibility
Minimum Age: 21 Years
Eligible Ages: ADULT, OLDER_ADULT
Sex: FEMALE
Healthy Volunteers: Yes
Locations
University of Alabama, Birmingham, Alabama, United States
Mobile OB/GYN, Mobile, Alabama, United States
Women's Health Research of Arizona, Phoenix, Arizona, United States
Quality of Life Medical & Research Center, Tucson, Arizona, United States
Visions Clinical Research, Tucson, Arizona, United States
Women's Health Care Research Corp., San Diego, California, United States
Blueskies Center for Women, Colorado Springs, Colorado, United States
Health Awareness Inc., Jupiter, Florida, United States
Altus Research, Lake Worth, Florida, United States
Segal Institute for Clinical Research, North Miami, Florida, United States
Miami Research Associates, South Miami, Florida, United States
Comprehensive Clinical Trails, LLC, West Palm Beach, Florida, United States
Medical Network for Education & Research, Decatur, Georgia, United States
Fellows Research Alliance - Savannah, Savannah, Georgia, United States
Women's Health Practice, Champaign, Illinois, United States
Indiana University, Indianapolis, Indiana, United States
Four Rivers Clinical Research, Paducah, Kentucky, United States
Louisiana State University, New Orleans, Louisiana, United States
BD 54 Loveton, Sparks, Maryland, United States
Saginaw Valley Medical Research, Saginaw, Michigan, United States
Virtua Phoenix OB/GYN, Moorestown, New Jersey, United States
Meridian Health / Jersey Shore University Medical Center, Neptune, New Jersey, United States
Quest Laboratories, Teterboro, New Jersey, United States
TriCore, Albuquerque, New Mexico, United States
Montefiore Medical Center, Bronx, New York, United States
Research Pathology Associates, LLC, Irvington, New York, United States
Eastern Carolina Women's Center, New Bern, North Carolina, United States
Lyndhurst Clinical Research, Winston-Salem, North Carolina, United States
HWC Women's Research Center, Englewood, Ohio, United States
Center for Women's Health of Lansdale, Lansdale, Pennsylvania, United States
Clinical Research of Philadelphia, Philadelphia, Pennsylvania, United States
Reading Health Physician Network, West Reading, Pennsylvania, United States
Fellows Research Alliance - Bluffton, Bluffton, South Carolina, United States
James T. Martin Jr. OB/GYN, North Charleston, South Carolina, United States
Chattanooga Medical Research, Chattanooga, Tennessee, United States
Center for Disease Detection, LLC, San Antonio, Texas, United States
Physicians Research Options, Draper, Utah, United States
Research Pathology Associates, Charlottesville, Virginia, United States
Tidewater Clinical Research, Virginia Beach, Virginia, United States
BioVision, Montréal, Quebec, Canada
Contact Details
Name: Tobi Karchmer, MD
Affiliation: Becton, Dickinson and Company
Role: STUDY_DIRECTOR
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