NCT02904915

Paracervical Block Versus No Paracervical Block During IUD Insertion

• Status: Completed
• Phase: Phase 4
• Study type: Interventional
• Enrollment: 50 (actual)
• Sponsor: The University of Texas Health Science Center, Houston · Academic / Other
• Sex: Female
• Age: 18 Years – 52 Years
• Healthy volunteers: Not accepted

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

Type	Name	Description
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.

Timeline

• Start date: 2017-01-12
• Primary completion: 2017-10-09
• Completion: 2017-10-09
• First posted: 2016-09-19
• Last updated: 2018-11-07
• Results posted: 2018-11-07

Locations

1 site across 1 country: United States

Regulatory

• FDA-regulated drug study