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Completed Phase 3 Interventional Results available

Study to Evaluate the Safety and Efficacy of ABT-712 in Subjects With Moderate to Severe Chronic Low Back Pain (CLBP)

ClinicalTrials.gov ID: NCT00761150

Public ClinicalTrials.gov record NCT00761150. 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 19, 2026, 6:02 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 3, Open-Label Period Followed by a Randomized, Double-blind, Placebo-controlled Study of the Analgesic Efficacy of Extended-release Hydrocodone/Acetaminophen (Vicodin CR) Compared to Placebo in Subjects With Chronic Low Back Pain

Brief summary

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

The primary purpose of the study was to test the efficacy of 2 tablets (twice daily) of ABT-712, compared to placebo, administered over a 4-week period in participants with moderate to severe mechanical chronic low back pain (CLBP).

Study identification

NCT ID
NCT00761150
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
AbbVie (prior sponsor, Abbott)
Industry
Enrollment
308 participants

Conditions and interventions

Interventions

Drug

Eligibility (public fields only)

Age range
21 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
Sep 2008 (Type not available)
Primary completion
Mar 2009 (Actual)
Completion
Mar 2009 (Actual)
Last update posted
Feb 7, 2014

2008 – 2009

United States locations

U.S. sites
32
U.S. states
13
U.S. cities
29
Facility City State ZIP Site status
Site Reference ID/Investigator# 10143 Tempe Arizona 85282 —
Site Reference ID/Investigator# 10161 Tempe Arizona 85282 —
Site Reference ID/Investigator# 10155 Tucson Arizona 85741 —
Site Reference ID/Investigator# 10160 Anaheim California 92801 —
Site Reference ID/Investigator# 10821 Lomita California 90717 —
Site Reference ID/Investigator# 10152 Clearwater Florida 33765 —
Site Reference ID/Investigator# 10157 DeLand Florida 32720 —
Site Reference ID/Investigator# 10142 Oldsmar Florida 34677 —
Site Reference ID/Investigator# 10147 Pembroke Pines Florida 33024 —
Site Reference ID/Investigator# 13821 Plantation Florida 33324 —
Site Reference ID/Investigator# 15821 Chicago Illinois 60611 —
Site Reference ID/Investigator# 10136 Crestview Hills Kentucky 41017 —
Site Reference ID/Investigator# 10822 New Orleans Louisiana 70114 —
Site Reference ID/Investigator# 10140 Shreveport Louisiana 71103 —
Site Reference ID/Investigator# 10158 Brockton Massachusetts 02301 —
Site Reference ID/Investigator# 13601 Fall River Massachusetts 02720 —
Site Reference ID/Investigator# 10162 Wellesley Hills Massachusetts 02481-2106 —
Site Reference ID/Investigator# 10159 Omaha Nebraska 68134 —
Site Reference ID/Investigator# 10126 Las Vegas Nevada 89144 —
Site Reference ID/Investigator# 10156 Cincinnati Ohio 45227 —
Site Reference ID/Investigator# 10148 Cincinnati Ohio 45242 —
Site Reference ID/Investigator# 10151 Kettering Ohio 45429 —
Site Reference ID/Investigator# 10138 Marion Ohio 43302 —
Site Reference ID/Investigator# 10150 Perrysburg Ohio 43554 —
Site Reference ID/Investigator# 10141 Dallas Texas 75251 —
Site Reference ID/Investigator# 10149 El Paso Texas 79902 —
Site Reference ID/Investigator# 10130 Fort Worth Texas 76135 —
Site Reference ID/Investigator# 10163 Killeen Texas 76543 —
Site Reference ID/Investigator# 13201 San Antonio Texas 78209-1744 —
Site Reference ID/Investigator# 10154 San Antonio Texas 78229 —
Site Reference ID/Investigator# 10144 Roanoke Virginia 24018 —
Site Reference ID/Investigator# 10113 Spokane Washington 99204 —

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 NCT00761150, 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 7, 2014 · Synced Oct 19, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00761150 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →