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临床试验/NCT00279903
NCT00279903已完成1 期

Intra-articular Botulinum Toxin Type-A in Knee Osteoarthritis - a Randomized, Cortisone Controlled, Double Blind Study.

Mayo Clinic1 个研究点 分布在 1 个国家目标入组 62 人开始时间: 2005年11月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
1 期
状态
已完成
发起方
Mayo Clinic
入组人数
62
试验地点
1
主要终点
Decrease in pain at 8 weeks post injection

研究概览

简要总结

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.

详细描述

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.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Double (Participant, Investigator)

入排标准

年龄范围
40 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • 未提供

排除标准

  • 未提供

研究组 & 干预措施

Cortisone

Active Comparator

干预措施: Cortisone (Drug)

Low Dose Btx-A

Experimental

干预措施: Botulinum toxin type A (Btx-A) (Drug)

High Dose Btx-A

Experimental

干预措施: Botulinum toxin type A (Btx-A) (Drug)

结局指标

主要结局

Decrease in pain at 8 weeks post injection

次要结局

  • Improvement in function at 2, 4, 8, 12, 26 weeks
  • Improvement in quality of life at 2, 4, 8, 12, 26 weeks
  • Decrease in pain at 2, 4, 12, 26 weeks

研究者

发起方
Mayo Clinic
申办方类型
Other

研究点 (1)

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