Home › NCT07846527

Vaginal Wall Retraction Using VuSleeve

Vaginal Wall Retraction in Gynecologic Exams and Procedures Using VuSleeve (Iris Study)

Who can join

Ages 21 to 65 · Women

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

About the study

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.

Sponsor: Ceek Women's Health, INC · Participants: 500 · Started: 2026-09

Contact the study team

• Tracy Bennett, MD · Phone: 855-559-2335

Official record on ClinicalTrials.gov — NCT07846527

Locations in the U.S.

From ClinicalTrials.gov, data retrieved Sep 30, 2026. Each study sets its own eligibility; the study team decides who can join.