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Clinical Trial Summary

The investigators theorize that the application of a lidocaine-prilocaine cream 5-10 minutes prior to the administration of a paracervical block could decrease pain associated with its administration and pain with abortion overall.


Clinical Trial Description

This is a superiority, double-blind randomized controlled trail of women ages 18 and older presenting for first-trimester surgical abortion. The lidocaine-prilocaine cream will be used in the experimental group in conjunction with a paracervical block, whereas plain lubricating gel will be used in conjunction with a paracervical block for the placebo, control group. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03508804
Study type Interventional
Source Stanford University
Contact
Status Withdrawn
Phase Phase 3
Start date December 2020
Completion date December 2022

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