Ketoprofen Topical Patch 20% in the Treatment of Pain Associated With Shoulder, Elbow or Knee Tendonitis or Bursitis - Full Text View

Sponsored by:	Endo Pharmaceuticals
Information provided by:	Endo Pharmaceuticals
ClinicalTrials.gov Identifier:	NCT00352625

Purpose

The purpose of this study is to evaluate the effect of a ketoprofen topical patch on the pain associated with tendonitis or bursitis of the shoulder, elbow or knee.

Condition	Intervention	Phase
Tendonitis Bursitis	Drug: Ketoprofen Topical Patch 20%	Phase III

Study Type:	Interventional
Study Design:	Treatment, Randomized, Double-Blind, Placebo Control, Parallel Assignment, Safety/Efficacy Study
Official Title:	A Randomized, Double-Blind, Placebo-Controlled, Parallel Group Phase III Study of the Efficacy, Tolerability and Safety of Ketoprofen Topical Patch, 20% (KTP) in the Treatment of Pain Associated With Tendonitis or Bursitis of the Shoulder, Elbow or Knee

Resource links provided by NLM:

MedlinePlus related topics: Bursitis

Drug Information available for: Ketoprofen

U.S. FDA Resources

Further study details as provided by Endo Pharmaceuticals:

Primary Outcome Measures:

Average pain intensity during daily activities

Secondary Outcome Measures:

Average pain intensity while at rest
Functional disability
Use of prn rescue medication
Quality of sleep
Patient's and physician's global assessments of study medication

Estimated Enrollment:	330
Study Start Date:	June 2006
Study Completion Date:	March 2007
Primary Completion Date:	February 2007 (Final data collection date for primary outcome measure)

Detailed Description:

This randomized, double-blind, placebo-controlled, parallel group study will be conducted in patients with tendonitis or bursitis of the shoulder, elbow or knee. Eligible patients will have tendonitis or bursitis or the shoulder, elbow or knee and will be randomized (in a 1:1 ratio) to receive double-blind treatment with either the KTP or a matching placebo patch to be applied once daily for 21 days. Patients will return to the clinic for assessments on Day 3, Day 7, Day 14 and Day 21; a follow-up assessment will be conducted by telephone on Day 35. At each visit through Day 21, patients will rate their average pain intensity during daily activities and while at rest using the 11-point scale (range 0 to 10), and will rate their functional disability. Patients will also complete an electronic diary in which pain intensity and pain relief ratings will be recorded three times daily. Ratings of the quality of sleep will be recorded in the diary each morning, and the use of study treatment and rescue medication will be recorded in the diary each day. Ibuprofen will be provided as prn rescue medication.

Eligibility

Ages Eligible for Study:	18 Years and older
Genders Eligible for Study:	Both
Accepts Healthy Volunteers:	No

Criteria

Inclusion

Males or females 18 years of age or older
Diagnosis of tendonitis or bursitis of the shoulder, elbow or knee
Meet pain entry criteria
Willing to discontinue use of any pain medication not provided by the study

Exclusion:

Have tendonitis or bursitis secondary to a systemic inflammatory disease, calcification or requiring surgery
Have received corticosteroids in the 30 days preceding screening
Have a history or physical examination finding that is incompatible with safe participation in the study
Have a history or physical examination finding that is incompatible with study product use
Are taking medications or other substances contraindicated due to the nature of the study medication or the potential for drug interactions.
Are taking medications that may significantly affect renal function

Contacts and Locations

Please refer to this study by its ClinicalTrials.gov identifier: NCT00352625

Locations

United States, Texas
PPD
Austin, Texas, United States, 78704

Sponsors and Collaborators

Endo Pharmaceuticals

Investigators

Principal Investigator:

PPD

PPD Austin, TX

More Information

No publications provided

Study ID Numbers:	EN3269-302
Study First Received:	June 30, 2006
Last Updated:	August 13, 2008
ClinicalTrials.gov Identifier:	NCT00352625 History of Changes
Health Authority:	United States: Food and Drug Administration

Keywords provided by Endo Pharmaceuticals:

Tendonitis
Bursitis
Pain
Shoulder Pain

Elbow Pain
Knee Pain
Tendon Injury
Muscle, Bone and Cartilage Disorders

Study placed in the following topic categories:

Anti-Inflammatory Agents
Ketoprofen
Tendon Injuries
Shoulder Pain
Joint Diseases
Cyclooxygenase Inhibitors
Wounds and Injuries
Disorders of Environmental Origin
Pain
Tendinopathy

Muscular Diseases
Musculoskeletal Diseases
Analgesics, Non-Narcotic
Cartilage Diseases
Anti-Inflammatory Agents, Non-Steroidal
Peripheral Nervous System Agents
Analgesics
Antirheumatic Agents
Bursitis

Additional relevant MeSH terms:

Anti-Inflammatory Agents
Ketoprofen
Tendon Injuries
Molecular Mechanisms of Pharmacological Action
Joint Diseases
Cyclooxygenase Inhibitors
Physiological Effects of Drugs
Wounds and Injuries
Disorders of Environmental Origin
Enzyme Inhibitors
Pharmacologic Actions
Tendinopathy

Muscular Diseases
Musculoskeletal Diseases
Analgesics, Non-Narcotic
Sensory System Agents
Therapeutic Uses
Anti-Inflammatory Agents, Non-Steroidal
Peripheral Nervous System Agents
Analgesics
Antirheumatic Agents
Central Nervous System Agents
Bursitis

ClinicalTrials.gov processed this record on July 02, 2009