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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
Phases
Phase 2Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00735124
Enrollment
5
Registered
2008-08-14
Start date
2008-11-06
Completion date
2009-09-30
Last updated
2017-04-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Analgesia, Hernia, Inguinal, Pain

Keywords

analgesia requirement and post operative pain

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

Interventions

DRUGGabapentin

1200 mg single dose gabapentin

OTHERplacebo

Injection of placebo/sham

Sponsors

University of Oklahoma
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 70 Years
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frameDescription
Post operative pain is reduced when single pre-operative oral dose of Gabapentine is given to the patient before the Inguinal Herniorrhaphy1yrsPost operative pain is reduced when single pre-operative oral dose of

Secondary

MeasureTime frameDescription
The post operative analgesia requirement is also reduced1yrsThe post operative analgesia requirement is also reduced

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026