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Efficacy of Intrauterine Lidocaine and Naproxen for Pain Control With Intrauterine Device Insertion

Pain Clinical Trial

Official title:
Efficacy of Intrauterine Lidocaine and Naproxen for Pain Control With Intrauterine Device Insertion

Clinical Trial Summary

To compare the efficacy of intrauterine lidocaine and oral naproxen sodium on discomfort and pain of patients undergoing intrauterine device insertion.

Clinical Trial Description

This is a randomized, double-blind, placebo-controlled study with women that will be recruited from our outpatient obstetrics and gynecology clinic. Women desiring intrauterine device insertion will be invited to participate.

The investigators plan to recruit women desiring intrauterine device insertion into one of four groups: A: placebo/normal saline infusion; B: placebo/lidocaine infusion; C: Saline infusion/ naproxen; D: lidocaine infusion/ naproxen. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT02769247
Study type Interventional
Source Walter Reed National Military Medical Center
Contact
Status Completed
Phase N/A
Start date June 2014
Completion date December 2016
View Details
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