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| Sponsor: | Abbott |
|---|---|
| Information provided by: | Abbott |
| ClinicalTrials.gov Identifier: | NCT00325949 |
Purpose
This is a study of the safety and pain-relieving ability of extended release hydrocodone and acetaminophen tablets in patients with moderate to severe low back pain
| Condition | Intervention | Phase |
|---|---|---|
|
Chronic Low Back Pain |
Drug: Extended release hydrocodone and acetaminophen (Vicodin CR) |
Phase III |
| Study Type: | Interventional |
| Study Design: | Treatment, Randomized, Double-Blind, Placebo Control, Parallel Assignment, Safety/Efficacy Study |
| Official Title: | A Phase 3, Open-Label Period Followed By a Randomized, Double-Blind, Placebo-Controlled Study of the Analgesic Efficacy and Safety of Extended Release Hydrocodone/Acetaminophen (Vicodin® CR) Compared to Placebo in Subjects With Chronic Low Back Pain |
| Estimated Enrollment: | 450 |
| Study Start Date: | May 2006 |
Eligibility| Ages Eligible for Study: | 21 Years to 75 Years |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria:
Exclusion Criteria:
Contacts and Locations
Show 62 Study Locations| Study Director: | Earle Lockhart, M.D. | Abbott |
More Information
| Study ID Numbers: | M05-790 |
| Study First Received: | May 11, 2006 |
| Last Updated: | October 24, 2007 |
| ClinicalTrials.gov Identifier: | NCT00325949 History of Changes |
| Health Authority: | United States: Food and Drug Administration |
|
Respiratory System Agents Nervous System Diseases Physiological Effects of Drugs Central Nervous System Depressants Low Back Pain Narcotics Pain Back Pain Pharmacologic Actions Signs and Symptoms Analgesics, Non-Narcotic |
Sensory System Agents Therapeutic Uses Hydrocodone Neurologic Manifestations Analgesics Peripheral Nervous System Agents Antitussive Agents Central Nervous System Agents Analgesics, Opioid Acetaminophen |