Clinical Trial

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

Completed
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Summary
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.
Protocol Amendment History 1 amendment
This ClinicalTrials.gov record has been amended once since 2026-01-09.
Trial Details
NCT Number NCT07351084
Lead Sponsor University of Kansas Medical Center
Conditions Intrauterine Device Complications, Contraceptive Device Failure, IUD Fragmentation, Retained Intrauterine Device, Female Contraception, Women's Health, Reproductive Health
Enrollment 44 participants
Start Date 2025-02-28
Primary Completion 2025-06-26 (estimated)
Study Completion 2025-06-26 (estimated)
Updated on ClinicalTrials.gov 2026-06-30