Vaginal Wall Retraction Using VuSleeve
Part of paid clinical trials in Aurora, Colorado.
- Sponsor
- Ceek Women's Health, INC
- Study ID
- NCT07846527
- Status
- Recruiting
Conditions
- Adult Females
Eligibility Criteria
- Sex
- FEMALE
- Age
- 21 Years - 65 Years
- Healthy Volunteers
- Not accepted
Study Details
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.
Key Dates
- First listed
- Sep 29, 2026
- Start date
- Sep 30, 2026
- Status verified
- Sep 2026
- Primary completion
- Dec 31, 2026
- Completion
- Dec 31, 2026
Study Design
- Enrollment
- 500 participants (estimated)
Arms
- Arm: Single Group
Primary Outcome Measure
Vaginal Sidewall Retraction [ Time Frame: Same day as previously scheduled gynecologic exam and/or procedure. ]
Central Contacts
- Tracy Bennett, MD855-559-2335
Locations (3)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| UCHealth Anschutz | Aurora | Colorado | 80045 | Christine Conageski, MD (PRINCIPAL_INVESTIGATOR) |
| Denver Health | Denver | Colorado | 80204 | Catherine Callinan, MD (PRINCIPAL_INVESTIGATOR) |
| Emory University | Atlanta | Georgia | 30322 | Lisa Flowers, MD, MPH (PRINCIPAL_INVESTIGATOR) Nadi Kaonga, MD (SUB_INVESTIGATOR) Mary Tadros, MD (SUB_INVESTIGATOR) |