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

Completed · Not applicable · Has a placebo group

Conditions studied: Contraception, Pain

In brief

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

Key facts

Study ID

NCT02769247

Run by

Walter Reed National Military Medical Center

People needed

160

Starts

2014-06-01

Expected to finish

2016-12-01

Last updated by the study team

2018-11-08

Who can join

Age: 18 and older. Sex: female. Healthy volunteers: accepted.

You may qualify if…

• DEERS-eligible reproductive age women (i.e. Tricare beneficiaries)
• age 18 years and older
• desiring Paragard or Mirena intrauterine device insertion

You may not qualify if…

• Current pregnancy
• cervical stenosis
• severe medical illness
• known allergy or sensitivity to lidocaine or naproxen
• peptic ulcer disease
• current pelvic inflammatory disease
• patients with known renal insufficiency
• patients using chronic NSAIDs or on chronic pain medication
• women desiring Skyla IUD insertion will also be excluded due to infrequency of insertions at WRNMMC

Where it is running

• Walter Reed National Military Medical Center — Bethesda, Maryland, United States

Full record on ClinicalTrials.gov

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