Diclofenac Patch for Treatment of Mild to Moderate Tendonitis or Bursitis

Cerimon Pharmaceuticals

Status and phase

Completed

Phase 3

Phase 2

Conditions

Subacromial Bursitis of the Shoulder

Medial Epicondylitis of the Elbow

Subdeltoid Bursitis of the Shoulder

Bicipital Tendonitis

Rotator Cuff Tendonitis

Lateral Epicondylitis of the Elbow

DeQuervain's Tenosynovitis of the Wrist

Treatments

Drug: Matching Placebo

Drug: diclofenac sodium

Study type

Interventional

Funder types

Industry

Identifiers

NCT00640939

DCF-003

Details and patient eligibility

About

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.

Full description

Cerimon Pharmaceuticals is investigating a topical patch formulation of diclofenac sodium containing 15 mg of diclofenac sodium for the local treatment of acute musculoskeletal pain.

Enrollment

308 patients

Sex

All

Ages

18 to 75 years old

Volunteers

No Healthy Volunteers

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