At a glance
ClinicalIndex Comparison RecordPhase 4Completed· 40 enrolled
Drug / intervention
Lidocaine +1 moredrug
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.
Double Blind, Randomized, Prospective Trial of Impact of Pain Scores on Intrauterine Lidocaine vs Normal Saline Infusion Before IUD Placement.
Women's Health Care Clinic, Torrance, California·interventional·Posted Mar 9, 2011·Updated Feb 5, 2014
In Brief
A Phase 4 clinical trial evaluating Lidocaine and Normal Saline for Pain. Completed, enrolled 40 participants across 1 site.
Detailed Summary
The study hypothesis is that infusion of 2% lidocaine at the time of IUD placement will reduce pain scores related to that procedure. In a double blinded randomized trial of 60 women receiving either normal saline or lidocaine infused through an endometrial aspirator, pain scores will be obtained for each step of the IUD placement procedure and for the total experience.
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsPain
CountriesUnited States
Collaborators--
Timeline
Phase 4CompletedFinished
20082009201020112012201320142015201620172018201920202021202220232024202520262027
Enrollment StartJul 2008
Primary CompletionDec 2008
First PostedMar 2011
Study CompletionDec 2012
TodayJul 2026
First PostedMar 9, 2011
Enrollment StartJul 1, 2008
Primary CompletionDec 1, 2008
Study CompletionDec 1, 2012
TodayJul 2, 2026
Enrollment to primary: 5 monthsPosted 15.3 years ago
Interventions
Lidocainedrug
1.33 cc 2% liquid lidocaine
Normal Salinedrug
1.33cc normal saline