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
| Type | Name | Description |
|---|---|---|
| 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 |
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.