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

• Status: Completed
• Trial end date: 2017-04-01
• Target enrollment: 0
• Participant gender: Female

Summary

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

• Phase: Phase 3
• Accepts Healthy Volunteers?: Accepts Healthy Volunteers

Details

• Lead Sponsor: Stanford University
• Treatments: Lidocaine

Criteria

Inclusion Criteria:

• 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

Exclusion Criteria:

• 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