IUD Clinical Trial - IUD Self-Removal Study

Status Recruiting

Clinical Trial 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.

Clinical Trial 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. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT05339555
Study type	Interventional
Source	Oregon Health and Science University
Contact	Women's Health Research Unit Department of Ob/Gyn
Phone	503-494-3666
Email	whru@ohsu.edu
Status	Recruiting
Phase	N/A
Start date	June 10, 2022
Completion date	December 31, 2024

View Details

See also
Status	Clinical Trial	Phase
Recruiting	`NCT03868137` - Multi-dose Ibuprofen Prophylaxis for IUD-insertion	N/A
Completed	`NCT04539899` - Evaluation of the Influence of the Virtual Reality Helmet on Pain During IUD Insertion	N/A
Recruiting	`NCT06023849` - Trans Caesarean Intra Uterine Contraceptive Device Insertion Versus Conventional Postpartum 6 Weeks Insertion	N/A
Completed	`NCT04932382` - Misoprostol Prior to Intrauterine Device Insertion	N/A
Active, not recruiting	`NCT04927741` - Essential Oils Following IUD Insertion	N/A
Completed	`NCT05383924` - Intrauterine Contraceptive Device Insertion During Cesarean Section (CS) Versus Delayed Insertion	N/A
Completed	`NCT04389021` - Virtual Reality Simulation for Intrauterine Device Insertion: A Randomized Clinical Trial	N/A
Completed	`NCT05187078` - Allis Clamp Versus Single-tooth Tenaculum	N/A
Completed	`NCT04379102` - The Role Of Local Anesthetics in the Management of Adverse Effects Associated With Intrauterine Device Application
Recruiting	`NCT05875571` - Intravenous Ketorolac Administration to Attenuate Post-procedural Pain Associated With Intrauterine Device Placement	Phase 4
Active, not recruiting	`NCT02076217` - Quick Start of Highly Effective Contraception
Recruiting	`NCT05700812` - IUD Placement Without Sounding	N/A
Recruiting	`NCT05252117` - Uterovaginal Plexus Block With Articaine for Intrauterine Device Placement Patients Who Are Indicated for the Use of Copper IUD as a Contraceptive Method Will be Invited to Participate in This Research.	Phase 4
Not yet recruiting	`NCT05471362` - Barriers of Immediate Postpartum Intrauterine Device Uptake
Not yet recruiting	`NCT04630548` - Safety and Efficacy of Immediate Post Placental IUD Insertion in Patients Undergoing Cesarean Delivery	N/A
Not yet recruiting	`NCT05283798` - Insertion of Copper T380 Versus Multiload IUD Post Partum	N/A
Not yet recruiting	`NCT06240260` - TENS Unit for Analgesia During IUD Insertion	N/A
Completed	`NCT06042556` - IUD Self-Removal: Evaluating an Online Guide for Self-removal in Clinical and Non-clinical Settings	N/A