Status:
COMPLETED
12 Versus 20 mL PCB for D&E Cervical Prep
Lead Sponsor:
Stanford University
Conditions:
Pain
Eligibility:
FEMALE
18+ years
Phase:
PHASE4
Brief 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 pla...
Detailed Description
This is a non-inferiority, single blinded, randomized controlled trial.This study will use a 2-site, 12 mL 1% plain lidocaine injection paracervical block (PCB) technique (2 mL for tenaculum placement...
Eligibility Criteria
Inclusion
- 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
- 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
Key Trial Info
Start Date :
January 1 2017
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
October 15 2020
Estimated Enrollment :
96 Patients enrolled
Trial Details
Trial ID
NCT03356145
Start Date
January 1 2017
End Date
October 15 2020
Last Update
January 23 2024
Active Locations (1)
Enter a location and click search to find clinical trials sorted by distance.
1
Stanford University
Stanford, California, United States, 94305