drugset / Trial / NCT01207401

Paracervical Block Before Intrauterine Device (IUD) Insertion

NCT01207401 ↗

Completed 50 enrolled Northwestern University
RandomizedParallel-groupOpen-labelTreatment

Summary

The purpose of this study is to evaluate if a paracervical block containing 1% lidocaine administered prior to IUD insertion reduces insertion pain. The hypothesis is that women receiving paracervical analgesia will experience less pain during IUD insertion than those who do not receive such analgesia.

Timeline

Start
2010-07
Primary completion
2011-02
Completion
2011-02

Drugs

EvaluationDrugModalityDoseRoute
Subject Lidocaine Other / unclassified 1 % Other

Indications

No indication recorded.