Use of Cervical Cap and Menstrual Disc for Application of Topical Anesthetic Prior to IUD Insertion

Recruiting N/A Interventional Study
IUD
No Placebo Group Every participant receives an active treatment — no one gets a placebo.
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At a Glance
Age
18 – 45
Sex
Female
Study type
Interventional
Purpose
Prevention
Participants needed
24 (estimated)
Sponsor
Oregon Health and Science University · Other
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About This Trial
This prospective, open label, double arm, feasibility group study will recruit participants planning to undergo office intrauterine device (IUD) placement without sedation or anxiolysis at the Center for Women's Health. Participants will self-administer a topical anesthetic using a contraceptive cervical cap or menstrual disc. Twenty-four nulliparous women will be recruited to receive one of two …
Trial Locations
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Eligibility Criteria
Inclusion Criteria: * Scheduled for IUD placement at the Center for Women's Health in Complex Family Planning clinic * Able to review and sign study consents in English * Generally healthy Exclusion Criteria: * History of any prior births, miscarriages, or abortions after 16 weeks' gestation * Cu…
Contacts

Women's Health Research Unit Department of Ob/Gyn

503-494-3666

whru@ohsu.edu

CONTACT