CI

At a glance

ClinicalIndex Comparison Record
Phase 4Completed· 50 enrolled
Drug / intervention
Lidocaine +2 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.

Search/NCT02904915
NCT02904915Phase 4Completed
CompareCT.gov

Paracervical Block Versus No Paracervical Block During IUD Insertion

The University of Texas Health Science Center, Houston·interventional·Posted Sep 19, 2016·Updated Nov 7, 2018

In Brief

A Phase 4 clinical trial evaluating Lidocaine, No analgesia, and 1 other intervention for Analgesia and IUD Insertion. Completed, enrolled 50 participants across 1 site.

Detailed Summary

The purpose of this study is to compare the pain level and level of discomfort with paracervical block versus no analgesia in women who present to the University of Texas (UT) Physicians Obstetrics and Gynecology Continuity Clinic, The UT Physicians Women's Center, and the UT Physicians Women's Center- Bellaire for IUD insertion.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsAnalgesia, IUD Insertion
CountriesUnited States
Collaborators--

Timeline

Phase 4CompletedFinished
2017201820192020202120222023202420252026
First PostedSep 19, 2016
Enrollment StartJan 12, 2017
Primary CompletionOct 9, 2017
TodayJul 2, 2026
Enrollment to primary: 9 monthsPosted 9.8 years ago

Interventions

Lidocainedrug

Intrauterine device (IUD) placement with paracervical block with 1% lidocaine.

No analgesiaother

IUD placement without analgesia.

Intrauterine device (IUD)device

IUD placement with or without paracervical block with 1% lidocaine.