Gabapentin in the Post-cesarean Pain Management of Buprenorphine Patient

Status Withdrawn

Clinical Trial Summary

The purpose of this study is to determine whether a perioperative course of gabapentin in parturients on buprenorphine maintenance would improve analgesia after elective cesarean delivery (CD).

Clinical Trial Description

Many strategies have been suggested to improve post-CD pain management in parturients on buprenorphine. While effective pain relief can be achieved, women maintained on buprenorphine during pregnancy have been shown to require up to 50% more opioids after CD compared to women with opioid use disorder not on a maintenance regimen. The perioperative use of gabapentin has been shown to reduce pain scores and opioid consumption following a variety of surgeries, ranging from cardiac bypass to total abdominal hysterectomy. The purpose of this study is to determine whether a perioperative course of gabapentin in parturients on buprenorphine maintenance would improve analgesia after elective CD. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT03335436
Study type	Interventional
Source	Vanderbilt University Medical Center
Contact
Status	Withdrawn
Phase	Phase 4
Start date	April 1, 2018
Completion date	December 2020

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