Rotator Cuff Tendonitis Clinical Trial
Official title:
A Randomized, Double-Blind, Placebo-Controlled Study of the Efficacy and Safety of a Diclofenac Sodium Patch for the Topical Treatment of Pain Due to Mild to Moderate Tendonitis or Bursitis
The primary purpose of this study is to assess the effectiveness of once daily application
of a diclofenac sodium patch to the skin near or over the painful area. In this study, the
location being studied will be one of the following: the affected shoulder, elbow, or wrist.
The secondary purpose of this study is to assess the safety and tolerability of the
diclofenac patch on the subject's skin, in the location being studied.
| Status | Completed |
| Enrollment | 308 |
| Est. completion date | June 2008 |
| Est. primary completion date | April 2008 |
| Accepts healthy volunteers | No |
| Gender | Both |
| Age group | 18 Years to 75 Years |
| Eligibility |
Inclusion Criteria: - 18 years to 75 years of age - Onset of painful upper extremity tendonitis or bursitis, no more than 21 days prior to study entry - Eligible diagnoses are rotator cuff tendonitis, bicipital tendonitis or subdeltoid/subacromial bursitis of the shoulder, medial or lateral epicondylitis of the elbow, and DeQuervain's tenosynovitis of the wrist - Spontaneous pain with motion or resisted motion and tenderness to palpation over the involved tendon(s), bursa, or epicondyle - Presence of pain of at least 5, with a maximum of 9, on an 11-point Numerical Rating Scale (NRS) Exclusion Criteria: - Aspirin, or short half-life NSAID use within 12 hours, or longer half-life NSAID use within 24 hours prior to study entry (see Appendix B: for table of NSAIDs) - Opioid use within 3 days prior to study entry - Topical treatment, other than local ice or heat, applied to the painful region within 3 days prior to study entry - History of peptic ulcer disease within 1 year prior to study entry, any history of gastrointestinal bleeding, or coagulation disorder - A history of, or evidence for underlying articular disease such as osteoarthritis, rheumatoid arthritis, gout, or pseudogout (calcium pyrophosphate deposition disease) - Clinically significant and poorly controlled pulmonary, gastrointestinal, hepatic, renal, endocrine, or cardiovascular disease - A history of hypersensitivity to diclofenac or diclofenac-containing products - A history of intolerance to acetaminophen (rescue medication in this trial) - A history of skin sensitivity to adhesives (e.g. adhesive tape) - Pregnant or breastfeeding women and women of child-bearing potential not using effective means of contraception |
Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Investigator), Primary Purpose: Treatment
| Country | Name | City | State |
|---|---|---|---|
| United States | PPD | Austin | Texas |
| Lead Sponsor | Collaborator |
|---|---|
| Cerimon Pharmaceuticals | PPD |
United States,
| Type | Measure | Description | Time frame | Safety issue |
|---|---|---|---|---|
| Primary | Assess the efficacy of diclofenac in subjects with tendonitis or bursitis of the shoulder, elbow, or wrist. | 14 days | No | |
| Secondary | Assess the safety and tolerability of diclofenac in subjects with tendonitis or bursitis of the shoulder, elbow, or wrist. | 14 days | No |
| Status | Clinical Trial | Phase | |
|---|---|---|---|
| Completed |
NCT01330641 -
Accuracy of Needle Placement Into The Subacromial Space of The Shoulder
|
N/A |