Status:
TERMINATED
Post-Operative Pain Scores and Analgesic Requirements After Elective Inguinal Herniorrhaphy
Lead Sponsor:
University of Oklahoma
Conditions:
Pain
Analgesia
Eligibility:
All Genders
18-70 years
Phase:
PHASE2
PHASE3
Brief 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...
Eligibility Criteria
Inclusion
- Subjects having elective surgery with open unilateral Inguinal herniorraphy
Exclusion
- Non elective surgery
- Patients currently on gabapentin therapy
- Patient hypersensitive to gabapentin surgery
- History of alcohol or drug abuse
- Patients who are pregnant or who are nursing
Key Trial Info
Start Date :
November 6 2008
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
September 1 2009
Estimated Enrollment :
5 Patients enrolled
Trial Details
Trial ID
NCT00735124
Start Date
November 6 2008
End Date
September 1 2009
Last Update
April 28 2017
Active Locations (1)
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1
OUHSC
Oklahoma City, Oklahoma, United States, 73152