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Development of a Pain Control Options Menu for IUD Insertion

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Duke University

Status

Enrolling

Conditions

IUD Insertion Pain

Treatments

Other: Pain control options menu

Study type

Interventional

Funder types

Other

Identifiers

NCT07278804
Pro00117230

Details and patient eligibility

About

The goal of this study is to evaluate if using a pain management options menu for IUD (intrauterine device) insertion improves patient autonomy, satisfaction, and/or pain. The main questions it aims to answer are:

Does a pain management options menu for IUD insertion improve patient autonomy? Does a pain management options menu for IUD insertion improve patient satisfaction? Does a pain management options menu for IUD insertion improve patient pain?

Researchers will compare survey data from patients receiving IUDs before and after a pain management options menu is implemented.

Participants will be asked to answer survey questions addressing their feelings of autonomy, satisfaction, and pain in regards to their IUD insertion experience.

Full description

The investigators are developing a pain management options menu to be given to patients who are undergoing IUD insertion with the goal of improving patient autonomy, satisfaction, and pain scores. The investigators will give patients a survey exploring these aspects of the IUD insertion experience and compare the survey results from patients who were surveyed before the menu was implemented and after the menu was implemented.

Enrollment

200 estimated patients

Sex

Female

Ages

18 to 50 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Having an IUD placed in a clinic visit
  • Able to read and speak English
  • Age 18-50 years old

Exclusion criteria

  • Having an IUD placed in the operating room under general anesthesia

Trial design

Primary purpose

Supportive Care

Allocation

Non-Randomized

Interventional model

Sequential Assignment

Masking

None (Open label)

200 participants in 2 patient groups

No menu - control group
No Intervention group
Description:
Control group - no intervention administered
Menu - intervention group
Experimental group
Description:
Participants will receive the pain control options menu prior to IUD insertion
Treatment:
Other: Pain control options menu

Trial contacts and locations

1

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Central trial contact

Emile Gleeson, MD; Elizabeth Thomason, MD, MPH

Data sourced from clinicaltrials.gov

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