Vaginal Dinoprostone Administration Prior to a T380A Intrauterine Device Insertion in Nulliparous Women.

Intrauterine Device Clinical Trial

Official title:
Effects of Prophylactic Vaginal Dinoprostone Administration Prior to a T380A Intrauterine Device Insertion in Nulliparous Women.

Status Completed

Clinical Trial Summary

To investigate whether vaginal dinoprostone administered before intrauterine device (IUD) insertion reduces failed insertions, insertion-related complications and pain in nulliparous women.

Clinical Trial Description

Women may experience pain and technical difﬁculties may be encountered when insertion of an intrauterine device (IUD) is attempted through a narrow cervical canal.IUD insertion- related complications and side effects are more common among women who had never delivered vaginally.n American College of Obstetricians and Gynecologists committee opinion encourages providers to use IUDs as a ﬁrst line of contraception in nulliparous women. ;

Study Design

Related Conditions & MeSH terms

Intrauterine Device

Clinical Trial Details

NCT number	NCT03686085
Study type	Interventional
Source	Cairo University
Contact
Status	Completed
Phase	Phase 3
Start date	September 30, 2018
Completion date	March 10, 2019

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See also
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