Trials / Terminated
TerminatedNCT00735124
Post-Operative Pain Scores and Analgesic Requirements After Elective Inguinal Herniorrhaphy
An Investigation of Post-Operative Pain Scores and Analgesic Requirements After Ambulatory Inguinal Herniorrhaphy With Pre-Operative Gabapentin Therapy
- Status
- Terminated
- Phase
- Phase 2 / Phase 3
- Study type
- Interventional
- Enrollment
- 5 (actual)
- Sponsor
- University of Oklahoma · Academic / Other
- Sex
- All
- Age
- 18 Years – 70 Years
- Healthy volunteers
- Not accepted
Summary
The study will investigate the effects of single dose pre-operative oral dose of gabapentin (1200) on post -operative pain scores and oral analgesic requirements.
Detailed description
The study will benefit patients in reducing post-operative pain scores as well as reduction in oral analgesic consumption. Gabapentin has been shown to reduce post operative pain pain scores in breast surgery, hysterectomy , spinal surgery, orthopedic and thyroid surgery
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Gabapentin | 1200 mg single dose gabapentin |
| OTHER | placebo | Injection of placebo/sham |
Timeline
- Start date
- 2008-11-06
- Primary completion
- 2009-09-01
- Completion
- 2009-09-01
- First posted
- 2008-08-14
- Last updated
- 2017-04-28
Locations
1 site across 1 country: United States
Source: ClinicalTrials.gov record NCT00735124. Inclusion in this directory is not an endorsement.