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Completed Phase 3 Interventional Results available

Surgical Pain After Inguinal Hernia Repair (SPAIHR)

ClinicalTrials.gov ID: NCT00551135

Public ClinicalTrials.gov record NCT00551135. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 24, 2026, 5:28 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Randomized, Double Blind Multi Center Dose Ranging Study Of The Efficacy And Safety Of Pregabalin Compared To Placebo In The Adjunctive Treatment Of Post Surgical Pain After Primary Inguinal Hernia Repair

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The purpose of this study is to test whether pregabalin added to the standard of care with dosing starting preoperatively and continuing for 1 week post surgery will decrease the intensity of acute post-operative pain following inguinal hernia repair.

Study identification

NCT ID
NCT00551135
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Enrollment
425 participants

Conditions and interventions

Eligibility (public fields only)

Age range
17 Years to 75 Years
Sex
Male
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Jan 2008 (Type not available)
Primary completion
Jun 2009 (Actual)
Completion
Sep 2009 (Actual)
Last update posted
Jan 25, 2021

2008 – 2009

United States locations

U.S. sites
24
U.S. states
10
U.S. cities
19
Facility City State ZIP Site status
Pfizer Investigational Site Birmingham Alabama 35235 —
Pfizer Investigational Site Glendale California 91206 —
Pfizer Investigational Site Laguna Hills California 92653 —
Pfizer Investigational Site Pasadena California 91105 —
Pfizer Investigational Site Lake Worth Florida 33462 —
Pfizer Investigational Site Pensacola Florida 32504 —
Pfizer Investigational Site Rochester Minnesota 55905 —
Pfizer Investigational Site Rochester New York 14642 —
Pfizer Investigational Site Stony Brook New York 11794-8480 —
Pfizer Investigational Site Durham North Carolina 27710 —
Pfizer Investigational Site Columbus Ohio 43210 —
Pfizer Investigational Site Pittsburgh Pennsylvania 15232 —
Pfizer Investigational Site Hermitage Tennessee 37075 —
Pfizer Investigational Site Hermitage Tennessee 37076 —
Pfizer Investigational Site Knoxville Tennessee 27920 —
Pfizer Investigational Site Knoxville Tennessee 37920 —
Pfizer Investigational Site Nashville Tennessee 37203 —
Pfizer Investigational Site Dallas Texas 75390-7208 —
Pfizer Investigational Site Houston Texas 77024 —
Pfizer Investigational Site Houston Texas 77054 —
Pfizer Investigational Site Houston Texas 77091 —
Pfizer Investigational Site Houston Texas 77098 —
Pfizer Investigational Site Humble Texas 77338 —
Pfizer Investigational Site Kingwood Texas 77339 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 18 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00551135, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Jan 25, 2021 · Synced Oct 24, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00551135 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →