NCT04204265CompletedNot Applicable
A Prospective Study of a Single Injection Cross-linked Sodium Hyaluronate (MONOVISC) to Provide Symptomatic Relief of Osteoarthritis of Shoulder Joint
Anika Therapeutics, Inc.4 sites in 2 countries25 target enrollmentStarted: December 17, 2019Last updated:
Conditions
Trial Snapshot
- Phase
- Not Applicable
- Status
- Completed
- Sponsor
- Anika Therapeutics, Inc.
- Enrollment
- 25
- Locations
- 4
- Primary Endpoint
- Numerical Rating Scale (NRS) Pain
Study Overview
Brief Summary
Obtain real world, post market data to confirm the clinical improvement and safety in patients treated with a single injection of MONOVISC for the symptomatic relief of osteoarthritis in the shoulder joint.
Detailed Description
The goal of this study is to demonstrate the clinical improvement and safety in patients treated with MONOVISC for shoulder osteoarthritis. Specifically, this study will provide confirmation to the effectiveness and safety of MONOVISC at relieving shoulder joint pain to 6 months post-treatment.
Study Design
- Study Type
- Interventional
- Allocation
- Na
- Intervention Model
- Single Group
- Primary Purpose
- Treatment
- Masking
- None
Eligibility Criteria
- Ages
- 18 Years to — (Adult, Older Adult)
- Sex
- All
- Accepts Healthy Volunteers
- No
Inclusion Criteria
- •Age 18 years or older
- •Body Mass Index (BMI) ≤ 45 kg/m2
- •Diagnosis of symptomatic osteoarthritic joint in the index joint (Kellgren Lawrence grade I to III or Guyette grade I to III) to be treated with MONOVISC injection.
- •Failed conservative treatment for joint osteoarthritis.
- •NRS pain ≥4 and ≤9 in the index joint.
- •Subject must be willing to abstain from other treatments of the index joint for the duration of the study.
- •Subject is willing to discontinue all analgesics including NSAIDs, except acetaminophen/paracetamol, at least seven days before the treatment injection and through the completion of the study.
- •Subject is willing to use only acetaminophen/paracetamol (up to a maximum of 4.0 grams per day per the package insert) for the treatment of joint pain for the duration of the study. At least forty-eight hours prior to the Baseline Visit and each follow-up visit, the subject is willing to discontinue use of acetaminophen/paracetamol.
- •Subject is willing to maintain a stable dose of oral glucosamine and/or chondroitin sulfate products throughout the study, if taken prior to signing the informed consent form (ICF).
- •Able and willing to provide signed informed consent.
Exclusion Criteria
- •History of hypersensitivity to any of the ingredients in the hyaluronan
- •Infection or skin disease in the area of the injection site or index joint
- •NRS pain > 3 in the contralateral joint
- •Subject received an injection of Hyaluronic Acid (HA) and/or steroid in either joint within 6 months of signing the informed consent form (ICF). A subject will be excluded if they are planning to receive an HA or steroid injection (other than the study injection) in either joint during the course of this study.
- •Known inflammatory or autoimmune disorders (including rheumatoid arthritis, gout), or other pre-existing medical conditions that, in the opinion of the investigator, could impact treatment of the index joint or affect the ability of the subject to accurately complete the study questionnaires and comply with the study requirements.
- •Subject is taking medications at the time of signing the ICF which could interfere with the treatment procedure, healing and/or assessments. This includes but is not limited to oral or injectable anticoagulant treatments, anti-aggregant platelet treatment, chronic opioid analgesics. Low dose aspirin used for cardiovascular protection is allowed if a stable regimen is maintained for the duration of the study.
- •Subjects who had an oral, intramuscular, intravenous, rectal suppository or topical (excluded in index joint only) corticosteroid prior 30 days of signing the ICF are excluded. Topical corticosteroid use at any site other than the index joint is allowed.
- •Significant trauma to the index shoulder within 26 weeks of screening
- •Chronic use of narcotics or cannabis.
- •Ligament instability or tear in index joint.
- •Diagnosis of fibromyalgia
- •Diagnosis of osteonecrosis in index joint
- •Uncontrolled diabetes with HbA1c of >7%.
- •Subject is a woman who is pregnant or breastfeeding at the Screening Visit or a woman of child bearing potential who refuses to use effective contraception during the course of the study.
- •Subject is receiving or in litigation for worker's compensation.
- •Otherwise determined by the investigator to be medically unsuitable for participation in this study.
Outcomes
Primary Outcomes
Numerical Rating Scale (NRS) Pain
Time Frame: From Baseline to 6 Months
Mean change in Numerical Rating Scale (NRS) Pain in the Index Shoulder from baseline to 6 Months post injection. NRS is an 11-Point scale where 0=No Pain, 10=Worst Pain. A larger negative value (maximum -10.0) for the change from baseline indicates less pain and a better clinical outcome following treatment.
Secondary Outcomes
- Disabilities of Arm, Shoulder & Hand (DASH) Index(From Baseline to 6 Months)
- Patient Global Assessment (PGA) Score(From Baseline to 6 Months)
- The Outcomes Measures for Rheumatic Arthritis Clinical Trials-Osteoarthritis Research Society International (OMERACT-OARSI) Responder Index(6 Months)
- Number of Participants NOT Using Rescue Medication (Acetaminophen/Paracetamol)(6 Months)
Investigators
Study Sites (4)
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