Overview

Effect of Paracervical Block Volume on Pain Control for Dilation and Curettage

Status:
Active, not recruiting
Trial end date:
2021-07-01
Target enrollment:
Participant gender:
Summary
The investigators are conducting a study on pain control for dilation and curettage (D&C). Participants are eligible to enroll if they are a planning to have a D&C in a participating clinic. The investigators are studying how different ratios of medication to liquid affect pain when injected around the cervix. Both potential methods use the same dose of medication, though researchers would like to know which one works better. To be in this study, participants must be over the age of 18 with an early pregnancy loss or undesired pregnancy measuring less than 12 weeks gestation undergoing D&C while awake in clinic.
Phase:
Phase 1
Details
Lead Sponsor:
University of California, San Diego
Collaborator:
University of California, Los Angeles
Treatments:
Arginine Vasopressin
Lidocaine
Vasopressins