Study on the association of uterine perforation and intrauterine device (IUD) expulsion with breastfeeding status at the time of IUD insertion and postpartum timing of IUD insertion in electronic medical record databases. A postmarketing requirement for Mirena (APEX IUD)

First published 04/02/2020

Last updated 02/07/2024

EU PAS number:

EUPAS33461

Study

Finalised

Download as PDF

Documents

Study protocol

Initial protocol

19682_Study Protocol_v1.0_2019-06-29_Redacted

English (708.64 KB - PDF) View document

Study results

19682_CSR abstract_v1.0_2020-11-11

English (356.07 KB - PDF) View document

Study report

Other information

ENCePP Seal

The use of the ENCePP Seal has been discontinued since February 2025. The ENCePP Seal fields are retained in the display mode for transparency but are no longer maintained.

Conflicts of interest of investigators

19682_CSR_v1.0_2020-11-11_Redacted

English (9.37 MB - PDF) View document

Study on the association of uterine perforation and intrauterine device (IUD) expulsion with breastfeeding status at the time of IUD insertion and postpartum timing of IUD insertion in electronic medical record databases. A postmarketing requirement for Mirena (APEX IUD)

Secondary tabs

Share this page