Patient Factors Associated With Fragmentation of Copper Intrauterine Device (IUD) Requiring Hysteroscopic Removal

University of Kansas Medical Center44 enrolled

Overview

The purpose of this retrospective chart review was to identify risks factors for patients associated to Cooper IUD fragmentation upon removal resulting in the requirement of a hysteroscopy evaluation.

Study Type

OBSERVATIONAL

Enrollment

Conditions

Intrauterine Device Complications Contraceptive Device Failure IUD Fragmentation Retained Intrauterine Device Female Contraception Women's Health Reproductive Health

Eligibility

Sex: FEMALE

Medical Language ↔ Plain English

Inclusion Criteria: * IUD removal and required hysteroscopy Exclusion Criteria: * Younger than 18 years old * IU removal without requiring hysteroscopy

Locations (1)

The University of Kansas Medical Center

Kansas City, Kansas, United States

Outcomes

Primary Outcomes

Number of Patients Who Underwent a Hysteroscopy Procedure Resulting From Intrauterine Device (IUD) Fragmentation Upon Removal

Identify patient risk factors for Cooper IDU fragmentation upon removal requiring a hysteroscopy by completing a retrospective chart review.

Time frame: January 2004- December 2024

Data from ClinicalTrials.gov

This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.