Independent directory Public ClinicalTrials.gov records United States
ClinicalTrials.gov record
Terminated Phase 4 Interventional

Lidocaine Patch 5% Versus Celecoxib 200 mg in Chronic Axial Low Back Pain

ClinicalTrials.gov ID: NCT00904397

Public ClinicalTrials.gov record NCT00904397. 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 21, 2026, 10:40 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, Open-Label Study Comparing the Efficacy and Safety of Lidocaine Patch 5% With Celecoxib 200 mg in Patients With Chronic Axial Low Back Pain

Brief summary

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

Patients who had axial lower back pain (LBP) with or without radiation present for at least 3 months and had daily moderate to severe LBP as the primary source of pain participated in a Phase IV clinical trial to assess the efficacy of lidocaine patch 5% compared to celecoxib 200 mg in treating chronic axial LBP with and without radiation.

Study identification

NCT ID
NCT00904397
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 4
Enrollment
98 participants

Conditions and interventions

Interventions

Drug

Eligibility (public fields only)

Age range
18 Years and older
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
Jul 2004 (Type not available)
Primary completion
Nov 2004 (Actual)
Completion
Not listed
Last update posted
Feb 15, 2010

Started 2004

United States locations

U.S. sites
21
U.S. states
14
U.S. cities
21
Facility City State ZIP Site status
Not listed Northport Alabama — —
Not listed Phoenix Arizona — —
Not listed Beverly Hills California — —
Not listed Encinitas California — —
Not listed San Diego California — —
Not listed Spring Valley California — —
Not listed Longwood Florida — —
Not listed North Miami Beach Florida — —
Not listed Plantation Florida — —
Not listed Chicago Illinois — —
Not listed Shreveport Louisiana — —
Not listed Boston Massachusetts — —
Not listed Berlin New Jersey — —
Not listed Bethpage New York — —
Not listed Tonawanda New York — —
Not listed Charlotte North Carolina — —
Not listed Dayton Ohio — —
Not listed Allentown Pennsylvania — —
Not listed Sellersville Pennsylvania — —
Not listed Greer South Carolina — —
Not listed Spokane Washington — —

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 NCT00904397, 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 Feb 15, 2010 · Synced Oct 21, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00904397 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →