Self-administered Lidocaine Gel for Pain-control During Cervical Preparation for Dilation and Evacuation

Completed · Phase 3

Conditions studied: Pain Management, Cervical Preparation

In brief

This study seeks to compare self-administered lidocaine gel for pain control during cervical preparation for dilation and evacuation (D\&E) to paracervical block.

Key facts

Study ID

NCT02852434

Run by

Stanford University

People needed

72

Starts

2016-07-01

Expected to finish

2017-04-01

Last updated by the study team

2019-06-07

Who can join

Age: 18 and older. Sex: female. Healthy volunteers: accepted.

You may qualify if…

• Women 18 and older
• Intrauterine pregnancy ≥16 weeks gestation
• English speaking competency
• Willing and able to sign consent forms
• Agree to comply with study procedures

You may not qualify if…

• Women less than 18 years of age
• IV conscious sedation
• Known allergy to study medication (lidocaine)
• Any women not meeting inclusion criteria above will be excluded from participation

Where it is running

• Stanford University — Palo Alto, California, United States

Full record on ClinicalTrials.gov

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