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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: NCT00763321

Public ClinicalTrials.gov record NCT00763321. 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 2, 2026, 5:39 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 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 is 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
NCT00763321
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
AbbVie (prior sponsor, Abbott)
Industry
Enrollment
287 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
Aug 31, 2008
Primary completion
Mar 31, 2009
Completion
Mar 31, 2009
Last update posted
Feb 5, 2014

2008 – 2009

United States locations

U.S. sites
31
U.S. states
20
U.S. cities
30
Facility City State ZIP Site status
Site Reference ID/Investigator# 10044 Huntsville Alabama 35801
Site Reference ID/Investigator# 10070 Burbank California 91505
Site Reference ID/Investigator# 10050 San Diego California 92108
Site Reference ID/Investigator# 10060 Atlantis Florida 33462
Site Reference ID/Investigator# 10069 Hollywood Florida 33023
Site Reference ID/Investigator# 10045 Kissimmee Florida 347411
Site Reference ID/Investigator# 10061 Tampa Florida 33603
Site Reference ID/Investigator# 10054 Atlanta Georgia 30327
Site Reference ID/Investigator# 10071 Marietta Georgia 30060
Site Reference ID/Investigator# 13604 Chicago Illinois 60654
Site Reference ID/Investigator# 10053 Evansville Indiana 47714
Site Reference ID/Investigator# 10055 Newburgh Indiana 47630
Site Reference ID/Investigator# 10043 Valparaiso Indiana 46383
Site Reference ID/Investigator# 10072 Prairie Village Kansas 66206
Site Reference ID/Investigator# 10041 Pasadena Maryland 21122
Site Reference ID/Investigator# 10049 Springfield Massachusetts 01103
Site Reference ID/Investigator# 10062 Biloxi Mississippi 39531
Site Reference ID/Investigator# 10066 Florissant Missouri 63031
Site Reference ID/Investigator# 10073 St Louis Missouri 63141
Site Reference ID/Investigator# 10056 Omaha Nebraska 68134
Site Reference ID/Investigator# 10075 Williamsville New York 14221
Site Reference ID/Investigator# 10065 Winston-Salem North Carolina 27103
Site Reference ID/Investigator# 10067 Fargo North Dakota 58104
Site Reference ID/Investigator# 10047 Oklahoma City Oklahoma 73103
Site Reference ID/Investigator# 10052 Altoona Pennsylvania 16602
Site Reference ID/Investigator# 10042 Bridgeville Pennsylvania 15017
Site Reference ID/Investigator# 10063 Greer South Carolina 29650
Site Reference ID/Investigator# 10046 Austin Texas 78705
Site Reference ID/Investigator# 10058 Austin Texas 78756
Site Reference ID/Investigator# 10059 Dallas Texas 75230
Site Reference ID/Investigator# 10048 Chesapeake Virginia 23320

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 NCT00763321, 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 5, 2014 · Synced Sep 2, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00763321 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →