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IUD Self-Removal Study

IUD Self-Removal: A Study to Pilot the Feasibility of a Novel Technique

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05339555
Enrollment
30
Registered
2022-04-21
Start date
2022-06-10
Completion date
2025-10-20
Last updated
2026-04-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

IUD

Keywords

IUD Removal

Brief summary

This is a pilot study designed to test the effectiveness of several techniques for intrauterine device (IUD) self-removal and to understand patient preferences regarding IUD self-removal and indicators of success as well as understanding the impacts of IUD self-removal on other clinical care.

Detailed description

The Investigators propose to test a novel method for self-removal of IUDs in an effort to increase the proportion of patients who are able to successfully and safely remove their IUD when desired. Participants will attempt self-removal in office, where a provider will be able to remove the IUD if unsuccessful. Participants will be instructed on current and novel techniques and the investigators will examine indicators of success as well as patient and provider preferences.

Interventions

OTHERInstructions for IUD Self-Removal Provided to Participant

The provider will offer any individual presenting for in-person IUD removal or exchange (removal-replacement) the option for self-removal. The participant will be provided a 'how to' instruction sheet with information on positioning and what to expect. The participant will first attempt removal with clean hands if desired, then utilizing non-sterile, clean gloves (not explicitly tested in prior studies) and if that fails, the use of a menstrual cup (a novel technique). If not successful, the provider will perform standard IUD removal in the clinic.

Sponsors

Oregon Health and Science University
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 50 Years
Healthy volunteers
Yes

Inclusion criteria

* Presenting at clinic for IUD removal or exchange * Willing and able to give consent with literacy in English or Spanish

Exclusion criteria

* Participants who are referred for a complicated IUD removal such as a stingless IUD, prior failed IUD removal attempt, or an IUD failure.

Design outcomes

Primary

MeasureTime frameDescription
Effectiveness of IUD Self-Removal TechniquesImmediately after IUD RemovalProportion of participants who successfully remove their IUDs

Countries

United States

Contacts

PRINCIPAL_INVESTIGATORJessica Reid, MD

Oregon Health and Science University

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Apr 28, 2026