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

Phase 2
Terminated
Conditions
Hernia, Inguinal
Analgesia
Pain
Interventions
Other: placebo
Registration Number
NCT00735124
Lead Sponsor
University of Oklahoma
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 surgery, hysterectomy , spinal surgery, orthopedic and thyroid surgery

Recruitment & Eligibility

Status
TERMINATED
Sex
All
Target Recruitment
5
Inclusion Criteria
  • Subjects having elective surgery with open unilateral Inguinal herniorraphy
Exclusion Criteria
  • 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

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
PlaceboplaceboPlacebo arm for blinding the medication
Single pre-op dose of GabapentineGabapentinActive treatment with the study drug
Primary Outcome Measures
NameTimeMethod
Post operative pain is reduced when single pre-operative oral dose of Gabapentine is given to the patient before the Inguinal Herniorrhaphy1yrs

Post operative pain is reduced when single pre-operative oral dose of

Secondary Outcome Measures
NameTimeMethod
The post operative analgesia requirement is also reduced1yrs

The post operative analgesia requirement is also reduced

Trial Locations

Locations (1)

OUHSC

🇺🇸

Oklahoma City, Oklahoma, United States

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