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Completed Phase 2 Interventional Results available

Dose-Ranging Study for Prolonged Postoperative Analgesia in Subject Undergoing Total Knee Arthroplasty

ClinicalTrials.gov ID: NCT00485693

Public ClinicalTrials.gov record NCT00485693. 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 Jul 21, 2026, 5:30 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 Phase 2 Multicenter, Randomized, Double-blind, Parallel-group, Active-control, Dose-ranging Study to Evaluate the Safety, Efficacy, and Comparative Systemic Bioavailability of a Single Administration of SKY0402 Via Local Infiltration for Prolonged Postoperative Analgesia in Subjects Undergoing Total Knee Arthroplasty.

Study identification

NCT ID
NCT00485693
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Pacira Pharmaceuticals, Inc
Industry
Enrollment
138 participants

Conditions and interventions

Interventions

  • Bupivacaine HCl Drug
  • SKY0402 Drug

Drug

Eligibility (public fields only)

Age range
18 Years to 75 Years
Sex
All
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
Jul 31, 2009
Completion
Jul 31, 2009
Last update posted
Jun 27, 2022

2007 – 2009

United States locations

U.S. sites
6
U.S. states
5
U.S. cities
6
Facility City State ZIP Site status
West Alabama Research, Inc. Birmingham Alabama 35209
California Clinical Research, Inc. Davis California 95616
Accurate Clinical Trials, Inc. Laguna Hills California 92653
St. Luke's Roosevelt Hospital New York New York 10019
The Ohio State University Medical Center Columbus Ohio 43220
Texas Tech University Health Science Center Lubbock Texas 79430

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 3 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00485693, 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 Jun 27, 2022 · Synced Jul 21, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00485693 live on ClinicalTrials.gov.

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