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Completed Phase 2 Interventional Results available

Dose-ranging Study for Postoperative Analgesia in Subjects Undergoing Primary Unilateral Inguinal Hernia Repair

ClinicalTrials.gov ID: NCT00485433

Public ClinicalTrials.gov record NCT00485433. 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 Sep 5, 2026, 8:04 AM 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 Phase 2 Multicenter, Randomized, Double-blind, Parallel-group, Active-control, Dose-ranging Study to Evaluate the Safety and Efficacy of a Single Administration of SKY0402 for Prolonged Postoperative Analgesia in Subjects Undergoing Primary Unilateral Inguinal Hernia Repair.

Brief summary

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

The purpose of this study is to evaluate three dose levels of SKY0402 compared with 105 mg of bupivacaine HCl.

Study identification

NCT ID
NCT00485433
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Pacira Pharmaceuticals, Inc
Industry
Enrollment
98 participants

Conditions and interventions

Interventions

Drug

Eligibility (public fields only)

Age range
18 Years and older
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
May 31, 2007
Primary completion
Nov 30, 2007
Completion
Jul 31, 2008
Last update posted
Mar 1, 2021

2007 – 2008

United States locations

U.S. sites
7
U.S. states
4
U.S. cities
6
Facility City State ZIP Site status
Arcadia Methodist Hospital Arcadia California 91007
Saddleback Valley Outpatient Surgery Laguna Hills California 92653
Huntington Memorial Hospital Pasadena California 91105
St. Luke's Roosevelt Hosptial Center New York New York 10025
Thomas Jefferson University Hospital Philadelphia Pennsylvania 19107
Memorial Hermann Healthcare System Houston Texas 77024
Kirby Outpatient Surgical Center Houston Texas 77054

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

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00485433, 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 Mar 1, 2021 · Synced Sep 5, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00485433 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →