About this trial
The goal of this study is to create a non-invasive diagnostic test to rule out gynecological cancer in females aged 45 and older with abnormal uterine or postmenopausal bleeding.
Eligibility criteria
Qualifiers
Evidence of a personally signed and dated informed consent form indicating that the subject has been informed of all pertinent aspects of the study.
Willing and able to comply with scheduled visits, study plan, and other procedures.
Expected to be available for the duration of the study and can be contacted by telephone during study participation.
Females aged 45 and older (with roughly 80% of enrolled subjects over the age of 50).
Disqualifiers
Investigator site staff members directly involved in the conduct of the study and their family members or subjects who are PinkDx, Inc. employees or their family members.
Other medical or psychiatric conditions that would increase the risk of study participation in the judgement of the Investigator.
Women who have had a hysterectomy.
Women with a known history of endometrial cancer or uterine sarcoma.
Trial design
Treatments tested in this trial
- Not listed