Gabapentin for Perioperative Pain Relief in Surgical Abortion

Status Completed

Clinical Trial Summary

Gabapentin preoperative use for evaluation of benefit to reduce pain during and after surgical office-based abortion.

Clinical Trial Description

A double-blind placebo controlled trial of gabapentin in the setting of an ambulatory surgical abortion center where patients receive either the routine intravenous sedation, local cervical anesthesia plus 600mg of gabapentin one hour prior to surgery vs. the same regimen plus placebo one hour prior to surgery. Our primary outcome measure will be post-operative validated pain scores using a 11-point visual analog scale (VAS). Secondary measures will include nausea and vomiting during, after and 24 hours after the procedure. A second and third pain assessment using VAS will be made at 30 minutes and at 24 hours postoperatively. ;

Study Design

Related Conditions & MeSH terms

Pain Control

Clinical Trial Details

NCT number	NCT04292171
Study type	Interventional
Source	University of Nevada, Las Vegas
Contact
Status	Completed
Phase	Early Phase 1
Start date	May 1, 2017
Completion date	March 30, 2018

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