A Study of Pain Relief in Osteoarthritis - Full Text View

Sponsor:	Abbott
Information provided by:	Abbott
ClinicalTrials.gov Identifier:	NCT00298974

Purpose

The purpose of this study is to compare the safety and pain-relieving ability of Vicodin CR to placebo in subjects with osteoarthritis (OA) of the hip or knee.

Condition	Intervention	Phase
Osteoarthritis	Drug: 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, Randomized, Multicenter, Double-Blind Study Comparing the Analgesic Efficacy of Extended Release Hydrocodone/Acetaminophen Tablets (Vicodin CR) to Placebo in Subjects With Osteoarthritis

Resource links provided by NLM:

MedlinePlus related topics: Osteoarthritis

Drug Information available for: Vicodin

U.S. FDA Resources

Further study details as provided by Abbott:

Primary Outcome Measures:

The mean absolute pain intensity difference from baseline to each subject's Week 12 evaluation

Secondary Outcome Measures:

Pain intensity difference from baseline to each scheduled evaluation
Proportion of treatment responders
Global assessments of study drug and arthritis status
Western Ontario and McMaster (WOMAC) Osteoarthritis Index total score and 3 subscales
SF-36v2 Health Status Survey

Estimated Enrollment:	800
Study Start Date:	February 2006

Eligibility

Ages Eligible for Study:	21 Years to 80 Years
Genders Eligible for Study:	Both
Accepts Healthy Volunteers:	No

Criteria

Inclusion Criteria:

Males and females ages 21 to 80
If female, must be of non-child bearing potential or practicing birth control
Has osteoarthritis of the hip or knee
Requires therapeutic doses of medication for osteoarthritis pain
Has sufficient pain to justify the use of around-the-clock opioids

Exclusion Criteria:

Is associated with any currently ongoing research study, or has previously participated in a Vicodin CR study
Is allergic to or has had a serious reaction to hydrocodone, other opioids, or acetaminophen
Cannot discontinue pain medications, even for the short time prior to the study start
Has any clinically significant illness or recent injury, or has any significant laboratory abnormality, or has recently had major surgery
Has a history of gastric bypass surgery or preexisting severe gastrointestinal narrowing, or history of diseases that may narrow the gastrointestinal tract
Has a history of malnutrition or starvation
Has a history of drug (licit or illicit) or alcohol abuse or addiction, or consumes more than 4 alcoholic drinks per day
Has a history of a major depressive episode within the past 2 years, or requires treatment with certain drugs for depression, or has a history of major psychiatric disorder
Pregnant or breastfeeding females
Is incapacitated, bedridden or confined to a wheelchair
Has initiated any new therapy or medication for OA within 1 month of screening
Has had surgery, certain types of procedures, or received certain medications for osteoarthritis within a specified time frame
Has other conditions that may cause pain, such as rheumatoid arthritis or gout

Contacts and Locations

Please refer to this study by its ClinicalTrials.gov identifier: NCT00298974

Show 83 Study Locations

Sponsors and Collaborators

Abbott

Investigators

Study Director:

Rita Jain, M.D.

Abbott

More Information

No publications provided

Study ID Numbers:	M04-697
Study First Received:	March 2, 2006
Last Updated:	October 24, 2007
ClinicalTrials.gov Identifier:	NCT00298974 History of Changes
Health Authority:	United States: Food and Drug Administration

Keywords provided by Abbott:

Osteoarthritis of the hip or knee

Additional relevant MeSH terms:

Musculoskeletal Diseases
Osteoarthritis
Joint Diseases
Arthritis
Rheumatic Diseases

ClinicalTrials.gov processed this record on February 08, 2010