NCT07846527Recruiting

Vaginal Wall Retraction Using VuSleeve

Ceek Women's Health, INC

Start Date

9/1/2026

Completion Date

12/1/2026

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.

Eligibility Criteria

Age Range: 21 years to 65 years

Inclusion Criteria: * Subject was assigned female at birth * Subject is 21 - 65 years of age, inclusive, at the time of exam or procedure * Subject is undergoing a gynecological exam and/or procedure * Subject has undergone one or more prior gynecological exams Exclusion Criteria: * Subject is pregnant * Subject has stated or documented history of vaginal dysplasia or vaginismus

Interested in This Trial?

Contact the trial locations directly using the information below to learn more about enrollment.

Expressing interest lets you review the study and consent before we connect you with the research site.

Conditions

Adult Females

Locations

UCHealth Anschutz

Aurora, Colorado 80045

United States

Denver Health

Denver, Colorado 80204

United States

Emory University

Atlanta, Georgia 30322

United States