Naproxen for Pain Control With Intrauterine Device Insertion

Status Completed

Clinical Trial Summary

The purpose of this study is:

1. To evaluate whether 550 mg of naproxen sodium reduces pain scores with IUD insertion on a 0-10cm visual analogue scale compared to placebo (primary outcome).

2. To evaluate whether 550 mg of naproxen sodium reduces pain scores with tenaculum placement, uterine sounding and post-procedurally on a 0-10 cm visual analog scale compared to placebo (secondary outcomes).

3. To establish if prophylactic naproxen sodium is acceptable for routine use prior to IUD insertion.

Hypothesis: The administration of naproxen sodium, 550mg orally, 1 hour prior to IUD insertion will lead to a reduction in pain scores associated with IUD insertion compared to placebo.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Contraception

Clinical Trial Details

NCT number	NCT02388191
Study type	Interventional
Source	Planned Parenthood League of Massachusetts
Contact
Status	Completed
Phase	N/A
Start date	April 2015
Completion date	April 2016

View Details

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