Last reviewed · How we verify

NCT07351084

Patient Factors Associated With Fragmentation of Copper Intrauterine Devices Requiring Hysteroscopic Removal

Completed Last updated 20 January 2026
What this trial tests

trial testing Hysteroscopy in Intrauterine Device Complications in 45 participants. Completed in 26 June 2025.

Timeline
28 February 2025
Primary endpoint
26 June 2025
26 June 2025

Quick facts

Lead sponsorUniversity of Kansas Medical Center
StatusCompleted
Study typeOBSERVATIONAL
Enrollment45
Start date28 February 2025
Primary completion26 June 2025
Estimated completion26 June 2025
Sites1 location across United States

Drugs / interventions tested

Conditions studied

Sponsor

University of Kansas Medical Center

Who can join

Adults 18 to 60, female only, with Intrauterine Device Complications or Contraceptive Device Failure. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

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.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

Verify or expand the search:

Other trials of Hysteroscopy

Trials testing the same drug.

Other University of Kansas Medical Center trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT07351084.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing