Clinical Research Directory

Inclusion Criteria: 1. Subjects aged \>=18 years at time of consent 2. Intended to undergo screening colposcopy 3. Considered by a physician or healthcare provider as being of "average risk" for cervical cancer 4. Willing to consent to blood draw cervical disease treatments 5. Willing to sonsent to follow-up for five years as per protocol Exclusion Criteria: 1. History of cervical cancer 2. History of any malignancy (patients who have undergone surgical removal of skin squamous cell cancer may be enrolled provided the procedure was completed at least 12 months prior to the date of provision of informed consent for the study) 3. Currently taking any anti-neoplastic or disease-modifying anti-rheumatic drugs. 4. Any major physical trauma (e.g. disruption of tissue, surgery, organ transplant, blood product transfusion) within the 30 days leading up to the provision of informed consent 5. Known medical condition which, in the opinion of the investigator, should preclude enrollment into the study