Periumbilical vibration during IUD insertion

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This randomized controlled trial compares pain during intrauterine device placement with and without a vibrating device applied to the umbilicus. Participants are assigned to receive the vibration or standard care and can use usual pain control methods. Pain is measured on a 1-100 scale at several points during the procedure, starting before the insertion. All procedures occur at Duke University, with English-speaking adults 18 and older eligible if scheduled for IUD insertion.

Why it matters

Who can join: the full rules

Inclusion Criteria:

* Age 18 years or older
* Capable of providing informed consent
* Scheduled for IUD insertion at either Duke 1J gynecology clinic or Family Planning clinic
* English-speaking

Exclusion Criteria:

* Currently pregnant
* Planned use of IV sedation during IUD placement
* Inability to provide informed consent due to disability or language barrier

Where it's running

• Duke University Hospital
  Durham, North Carolina, United States Recruiting

Study contacts

• Principal investigator: Beverly Gray, MD — Duke Health
• Study coordinator: Madeline Thornton, MD, MPH
• Email: madeline.thornton@duke.edu
• Phone: (919) 668- 2591

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.