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Vaginal Wall Retraction Using VuSleeve
Sponsor: Ceek Women's Health, INC
Summary
This is a post-market, observational, non-interventional, single group/cohort study in which participants already have a scheduled gynecological exam and/or procedure. The goal of this study is to obtain investigator perspectives on using VuSleeve for routine gynecological care. Investigator perspectives from this mixed-method study will be captured through quantitative and qualitative components.
Official title: Vaginal Wall Retraction in Gynecologic Exams and Procedures Using VuSleeve (Iris Study)
Key Details
Gender
FEMALE
Age Range
21 Years - 65 Years
Study Type
OBSERVATIONAL
Enrollment
500
Start Date
2026-09
Completion Date
2026-12
Last Updated
2026-09-29
Healthy Volunteers
Not specified
Conditions
Locations (3)
UCHealth Anschutz
Aurora, Colorado, United States
Denver Health
Denver, Colorado, United States
Emory University
Atlanta, Georgia, United States