MedTrace Logo

Administration of Pre-Operative Gabapentin to Patients Undergoing Laparoscopy

NCT02359110 · Status: COMPLETED · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 112

Last updated 2018-03-12

Study results available
· View outcomes & findings →

Summary

The purpose of this study is to prospectively determine the influence of immediate pre-operative gabapentin administration on acute postoperative pain. The investigators hypothesize that immediate post-operative pain will be improved with pre-operative administration of gabapentin.

Conditions

  • Postoperative Pain

Interventions

DRUG

Gabapentin

Patients will receive Gabapentin 300mg tab less than 1 hour before surgery.

OTHER

Placebo

Patient will receive placebo tab less than 1 hour before surgery

Sponsors & Collaborators

  • Milton S. Hershey Medical Center

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
TRIPLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
80 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2015-06-30
Primary Completion
2017-01-31
Completion
2017-01-31

Countries

  • United States

Study Locations

More Related Trials

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02359110 on ClinicalTrials.gov