MedTrace Logo

Paracervical Block Versus No Paracervical Block During IUD Insertion

NCT02904915 · Status: COMPLETED · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 50

Last updated 2018-11-07

Study results available
· View outcomes & findings →

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.

Conditions

  • Analgesia
  • IUD Insertion

Interventions

DRUG

Lidocaine

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

OTHER

No analgesia

IUD placement without analgesia.

DEVICE

Intrauterine device (IUD)

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

Sponsors & Collaborators

  • The University of Texas Health Science Center, Houston

    lead OTHER

Principal Investigators

  • Pamela D Berens, MD · The University of Texas Health Science Center, Houston

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
52 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2017-01-12
Primary Completion
2017-10-09
Completion
2017-10-09
FDA Drug
Yes

Countries

  • United States

Study Locations

More Related Trials

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02904915 on ClinicalTrials.gov