The Use of a Novel Vaginal Speculum for Endometrial Biopsies

Enrolling by invitation · Not applicable

Conditions studied: Endometrial Cancer

In brief

The objective of this clinical trial is to determine if a newly-designed and FDA-cleared vaginal speculum (the Bouquet Speculum) will provide better visualization of the cervical os, be easier and more efficient to use, provide more consistent outcomes and decrease the discomfort associated with endometrial biopsy procedures.

Key facts

Study ID

NCT07217353

Run by

Rocky Vista University, LLC

People needed

100

Starts

2026-02-15

Expected to finish

2026-09-30

Last updated by the study team

2026-06-18

Who can join

Age: 18 and older, up to 90. Sex: female. Healthy volunteers: not accepted.

You may qualify if…

• Biological women with a uterus, age 18-90
• Previous endometrial biopsy procedure performed at the Minnesota Oncology Clinic

You may not qualify if…

• Pregnant women, active pelvic infection, or uncontrolled bleeding dyscrasias as determined by the provider at Minnesota Oncology Clinics
• Biological women without a uterus who are less than 18 years old or greater than 90 years old, or who have not had a previous endometrial biopsy at the Minnesota Oncology Clinic.

Where it is running

• Rocky Vista Health Clinic — Englewood, Colorado, United States

Full record on ClinicalTrials.gov

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