12 Versus 20 mL PCB for D&E Cervical Prep

• Status: Completed
• Trial end date: 2020-10-15
• Target enrollment: 0
• Participant gender: Female

Summary

More research is needed to investigate methods of pain control for cervical preparation for abortion procedures. Women report pain with paracervical block injection as well as with osmotic dilator placement. This study seeks to compare a 12 mL, 2-site 1% plain lidocaine paracervical block for pain control during cervical preparation (osmotic dilator insertion) for Dilation and Evacuation (D&E) to a 20 mL 1% lidocaine 2-site paracervical block.

• Phase: Phase 4
• Accepts Healthy Volunteers?: Accepts Healthy Volunteers

Details

• Lead Sponsor: Stanford University

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