Is Botox Effective in Relieving Pain From Knee Osteoarthritis?

Mayo Clinic

Status and phase: Completed; Phase 1

Conditions: Osteoarthritis, Knee

Treatments: Drug: Cortisone; Drug: Botulinum toxin type A (Btx-A)

Study type: Interventional

Funder types: Other

Identifiers

NCT00279903

1565-05

Details and patient eligibility

About

Patients with painful knee osteoarthritis will be randomly allocated to one of three groups. Each group will receive a knee injection of: 1) cortisone, 2) low dose Botox, or 3) high dose Botox. Patients will then be followed for 6 months to see if they have significant pain relief or improvement in their activity level after the injection.

Full description

Abstract Botulinum toxin type A (Btx-A) has been extensively studied and used clinically for its muscle paralyzing effects, but there is a growing body of evidence to support a role in pain modulation. Symptomatic osteoarthritis is a leading cause of pain, functional impairment, and disability, with significant indirect costs to society. Preliminary evidence suggests that Btx-A has a significant nociceptive effect, when injected intra-articularly, in to painful joints. The proposed study will evaluate the efficacy and safety of Btx-A injected intra-articularly in 60 subjects with moderate pain and functional impairment secondary to knee osteoarthritis, in a randomized, cortisone-controlled, double blind study, over a 6 month follow up period. If Btx-A is shown to be of equal or greater efficacy than cortisone in this patient population, it may be an excellent second line treatment for osteoarthritis, in multiple joints, where surgery is contraindicated or deferred due to age, comorbidities, or patient preference. Further studies examining the mechanism of action at the biochemical level, the clinical effect of Btx-A in other joints (in both osteoarthritis and inflammatory arthritis), the efficacy of Btx-A compared to hyaluronic acid (the only currently available injectable alternative to cortisone), and the side effect profile (effect on adjacent muscle strength, joint position sense, and long-term outcomes) would be indicated.

Enrollment: 62 patients

Sex: All

Ages: 40+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

1. A history of knee joint pain for greater than 6 months.
2. Medial or lateral tibiofemoral joint line tenderness.
3. Unilateral knee pain 6/10 or greater, on average, on the visual analog scale (VAS), that interferes with function most days per week.
4. Prior failed treatment with acetaminophen and/or non steroidal anti-inflammatory medications, and physical therapy (quadriceps strengthening).
5. Kellgren grade II or III radiographic changes of osteoarthritis.

Exclusion criteria

1. Age less than 40 years.
2. Anticoagulation with warfarin or heparin.
3. Known allergy or sensitivity to any of the components of the study medications.
4. Body mass index greater than 35.
5. Previous major reconstructive surgery on the affected knee.
6. Previous arthroscopic surgery on the affected knee in the past 12 months.
7. History of crystal induced arthropathy.
8. Use of aminoglycoside antibiotics, curare-like agents, or history of neuromuscular disease such as myasthenia gravis, amyotrophic lateral sclerosis, or myopathy.
9. History of or evidence of active rheumatologic disease, diabetes, severe peripheral neuropathy, clinically evident cardiac or respiratory disease that interferes with functional status, or other serious diseases, including psychiatric disorders.
10. Evidence of recent alcohol or drug abuse, or history of medication misuse or addiction.
11. Females who are pregnant, breastfeeding, or planning a pregnancy during the study, or who think that they may be pregnant at the start of the study, or females of childbearing potential who are unable or unwilling to use a reliable form of contraception during the study.
12. Intra-articular (knee) or systemic steroids in the past 6 months, or intra-articular knee hyaluronic acid injection in the past 6 months.
13. Patients who rate their average daily pain as less than 6 on a 10 point VAS scale at the screening visit.
14. Concurrent participation in another investigational drug or device study or participation in the 30 days immediately prior to study enrollment.

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Double Blind

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62 participants in 3 patient groups

Cortisone

Active Comparator group

Treatment:

Drug: Cortisone

Low Dose Btx-A

Experimental group

Treatment:

Drug: Botulinum toxin type A (Btx-A)

High Dose Btx-A

Experimental group

Treatment:

Drug: Botulinum toxin type A (Btx-A)