Actively Recruiting

Phase Not Applicable
Age: 18Years - 45Years
FEMALE
Healthy Volunteers
NCT05254041

Pilot Study of Suction as a Mechanism of IUD Expulsion With Concomitant Menstrual Cup Use

Led by University of Colorado, Denver · Updated on 2026-02-12

80

Participants Needed

1

Research Sites

253 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This study will provide pilot data examining suction as a mechanism of IUD displacement with menstrual cup use. The investigator hypothesize that manufacturer-recommended menstrual cup insertion and removal by breaking the seal will result in 15% rate of IUD displacement/expulsion. The investigator will also use this data to explore variables associated with IUD displacement and menstrual cup use. By examining the role of suction as a possible mechanism of IUD displacement, this research will allow healthcare providers to better counsel patients who use IUDs regarding menstrual cup use. Having a better understanding of the mechanics of IUD displacement could lead to the development of strategies to prevent expulsion.

CONDITIONS

Official Title

Pilot Study of Suction as a Mechanism of IUD Expulsion With Concomitant Menstrual Cup Use

Who Can Participate

Age: 18Years - 45Years
FEMALE
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Female
  • Between the ages of 18 and 45
  • Currently has an FDA approved IUD
  • Presenting to CWHC for IUD removal
Not Eligible

You will not qualify if you...

  • Known sensitivity or allergy to silicone
  • Known active vaginal infection (yeast, bacterial vaginosis, untreated sexually transmitted infection)
  • IUD strings not visible
  • Positive pregnancy test

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Comprehensive Women's Health Center

Denver, Colorado, United States, 80230

Actively Recruiting

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Research Team

C

Cara Clure, MD

CONTACT

E

Eva Dindinger, MPH

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

OTHER

Number of Arms

1

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