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Completed Phase 2 Interventional

Study of the Efficacy and Safety of Bupivacaine TTS Patch in Patients With Chronic Low Back Pain

ClinicalTrials.gov ID: NCT01096966

Public ClinicalTrials.gov record NCT01096966. 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 3, 2026, 3:39 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 12-Week, Randomized, Double-Blind, Placebo-Controlled, Parallel Group Study of the Efficacy and Safety of Bupivacaine TTS (Bupivacaine Patch) in Patients With Chronic Low Back Pain

Brief summary

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

This study will evaluate the efficacy and safety of Bupivacaine TTS (Bupivacaine patch) compared to placebo in patients with chronic low back pain.

Study identification

NCT ID
NCT01096966
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Durect
Industry
Enrollment
263 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years to 70 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
Feb 28, 2010
Primary completion
Jan 31, 2011
Completion
Jan 31, 2011
Last update posted
Jun 14, 2022

2010 – 2011

United States locations

U.S. sites
21
U.S. states
12
U.S. cities
21
Facility City State ZIP Site status
Not listed Tempe Arizona 85283
Not listed La Mesa California 91942
Not listed Torrance California 90502
Not listed Fort Lauderdale Florida 33306
Not listed Gainesville Florida 32605
Not listed Longwood Florida 32779
Not listed West Palm Beach Florida 33409
Not listed Marietta Georgia 30060
Not listed Newnan Georgia 30265
Not listed Springfield Massachusetts 01103
Not listed St Louis Missouri 63141
Not listed New York New York 10004
Not listed Winston-Salem North Carolina 27103
Not listed Oklahoma City Oklahoma 73109
Not listed Allentown Pennsylvania 18103
Not listed Altoona Pennsylvania 16602
Not listed Philadelphia Pennsylvania 19139
Not listed Austin Texas 78756
Not listed Dallas Texas 75231
Not listed Houston Texas 77074
Not listed Richmond Virginia 23294

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 NCT01096966, 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 14, 2022 · Synced Sep 3, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01096966 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →