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Self-administered Lidocaine Gel for Pain-control During Cervical Preparation for Dilation and Evacuation | Clinical Trials | Clareo Health

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COMPLETEDPhase 3NCT02852434

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

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

Lead sponsor: Stanford University•1 U.S. locations•View source on ClinicalTrials.gov

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Trial snapshot

StatusCOMPLETED

PhasePHASE3

Enrollment72

Start dateJul 2016

Last updatedJun 7, 2019

Condition

Pain Management, Cervical Preparation

Locations shown

Stanford University

Palo Alto, California

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Data Source & Attribution

This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.

ClinicalTrials.gov last update: June 7, 2019Data synced to Clareo: May 3, 2026

Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.

Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.

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