Post-Operative Pain Scores and Analgesic Requirements After Elective Inguinal Herniorrhaphy

Stopped early · Phase 2/Phase 3 · Has a placebo group

Conditions studied: Pain, Analgesia, Hernia, Inguinal

In brief

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.

Key facts

Study ID

NCT00735124

Run by

University of Oklahoma

People needed

5

Starts

2008-11-06

Expected to finish

2009-09-01

Last updated by the study team

2017-04-28

Who can join

Age: 18 and older, up to 70. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Subjects having elective surgery with open unilateral Inguinal herniorraphy

You may not qualify if…

• 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

Where it is running

• OUHSC — Oklahoma City, Oklahoma, United States

Full record on ClinicalTrials.gov

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