CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 50 enrolled
Drug / intervention
Lidocainedrug
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT01207401
NCT01207401N/ACompleted
CompareCT.gov

Pain Control for Intrauterine Device Insertion: A Randomized Trial of 1% Lidocaine Paracervical Block

Northwestern University·interventional·Posted Sep 22, 2010·Updated Jun 10, 2013

In Brief

A clinical study evaluating Lidocaine for Pain Control for Intrauterine Device Insertions. Completed, enrolled 50 participants across 1 site.

Detailed 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.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsPain Control for Intrauterine Device Insertions
CountriesUnited States
Collaborators--

Timeline

N/ACompletedFinished
2011201220132014201520162017201820192020202120222023202420252026
First PostedSep 22, 2010
Enrollment StartJul 1, 2010
Primary CompletionFeb 1, 2011
TodayJul 2, 2026
Enrollment to primary: 7 monthsPosted 15.8 years ago

Interventions

Lidocainedrug

1% Lidocaine