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RECRUITING
NCT07846527

Vaginal Wall Retraction Using VuSleeve

Sponsor: Ceek Women's Health, INC

View on ClinicalTrials.gov

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