Clinical Trials Directory

Trials / Completed

CompletedNCT02359110

Administration of Pre-Operative Gabapentin to Patients Undergoing Laparoscopy

Administration of Pre-Operative Gabapentin to Patients Undergoing Laparoscopy: A Prospective Double-blinded, Placebo Controlled Randomized Study

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
112 (actual)
Sponsor
Milton S. Hershey Medical Center · Academic / Other
Sex
Female
Age
18 Years – 80 Years
Healthy volunteers
Accepted

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.

Detailed description

The purpose of this study is to prospectively determine the influence of immediate pre-operative gabapentin administration on acute postoperative pain. We hypothesize that immediate post-operative pain will be improved with pre-operative administration of gabapentin. We plan to conduct a prospective randomized trial to assess the effect of a single immediate pre-operative dose of gabapentin 300mg on immediate post-operative pain in patients undergoing laparoscopy for gynecologic indications. This concept has been studied in patients undergoing abdominal hysterectomy. We aim to study the effect on patients undergoing laparoscopy.

Conditions

Interventions

TypeNameDescription
DRUGGabapentinPatients will receive Gabapentin 300mg tab less than 1 hour before surgery.
OTHERPlaceboPatient will receive placebo tab less than 1 hour before surgery

Timeline

Start date
2015-06-01
Primary completion
2017-01-01
Completion
2017-01-01
First posted
2015-02-09
Last updated
2018-03-12
Results posted
2018-03-12

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT02359110. Inclusion in this directory is not an endorsement.