Clinical Trials Directory

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

TypeNameDescription
DRUGGabapentin1200 mg single dose gabapentin
OTHERplaceboInjection 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.