Overview
This purpose of this research study is to determine the effectiveness of the Personal Pap Smear Device™ to collect adequate cervical cell samples for cytology examination when compared with the Rover Cervex-Brush (Cervix-Examination Brush).
Description
To determine the effectiveness of the Personal Pap Smear Device™ to collect adequate (as defined by Bethesda Guidelines 2014) cervical cell samples for cytology examination as compared with the Rover Cervex-Brush (Cervix-Examination Brush).
Eligibility
Inclusion Criteria:
- Adult women, aged 21-65 years old.
- Do not have any medical or psychiatric condition affecting the ability to give voluntary informed consent.
- Be able to read and understand English
Exclusion Criteria:
- Participants currently on menses
- Inability to provide Informed Consent
- Previous total hysterectomy
- History of radiation treatment for cervical cancer
- Pregnancy
- Medical condition that interferes with conduct of study, in investigator's opinion
- Evidence of active cervical infection requiring treatment
- Known bleeding diathesis