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临床试验/NCT02829281
NCT02829281Unknown4 期

Intra-articular Botulinum Toxin Type A Versus Corticosteroids: a Clinical Trial in Osteoarthritis of Knees

Federal University of São Paulo1 个研究点 分布在 1 个国家目标入组 105 人开始时间: 2016年7月最近更新:
适应症
干预措施

试验速览

阶段
4 期
发起方
入组人数
105
试验地点
1
主要终点
Changes on Pain

研究概览

简要总结

Introduction: Osteoarthritis of the knee is a very common disease. However there are few treatment options for these patients. Botulinum toxin type A is an option for chronic pain. If the investigators prove effectiveness of its use for intra-articular analgesia, Botulinum toxin type A can be useful for treat these patients.

Objective: Compare the effectiveness of the use of intra-articular corticosteroid versus Botulinum toxin type A in the treatment of patients with knee osteoarthritis.

Methods: A prospective controlled randomized double blind studied with three groups (n = 35 each group) of patients with symptomatic osteoarthritis of the knees receive intra-articular medication in a single moment will be undertaken. The three groups will be: Botulinum toxin type A Group: patients who receive 100 units of botulinum toxin; hexacetonide of triamcinolone Group: patients who receive 40mg of triamcinolone hexacetonide, and saline group: patients who receive 2ml of normal saline. Patients will be assessed by evaluators " blind " in 4 times during 12 weeks of follow-up with clinical assessment instruments (pain, quality of life questionnaire as short form 36 questionnaire) , functional ( WOMAC questionnaire) , and ultrasound (quantitative and semi quantitative measure of synovial hypertrophy and semi quantitative Power Doppler ) .The following statistical tests will be used : Student's t test, Mann - Whitney , chi- square test and ANOVA for repeated measures . Will be considered as statistical significance the difference of 5 %.

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, Outcomes Assessor)

入排标准

年龄范围
50 Years 至 80 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • age above 50 years
  • diagnose of knee osteoarthritis using clinics and radiographic criteria
  • pain for more than 6 months
  • analogic visual scale among 4 to 8
  • patients who agree to sign informed consent

排除标准

  • secondary osteoarthritis
  • skin lesion
  • use of intraarticular corticosteroid in the last 3 months
  • use of oral corticosteroid in the last 30 days
  • Kellgren Lawrence I or IV
  • inflammatory arthritis
  • neuromuscular disease
  • use of aminoglycoside antibiotics
  • metalic prosthesis in knee
  • peripheric neuropathy
  • serious cardiovascular or pulmonary disease
  • serious disorder of coagulation
  • pregnancy or breastfeeding
  • infections
  • use of wheelchair

研究组 & 干预措施

Botulinum toxin group

Experimental

Patients will receive a intervention with joint injection of 100 units of botulinum toxin

干预措施: Botulinum Toxin Type A (Drug)

Corticosteroid group

Active Comparator

Patients will receive a intervention with joint injection of 40mg of triamcinolone hexacetonide (corticosteroid)

干预措施: Triamcinolone hexacetonide (Drug)

Saline Group

Placebo Comparator

Patients will receive a joint injection of 2ml of normal saline

干预措施: Saline (Drug)

结局指标

主要结局

Changes on Pain

时间窗: Baseline, after 4, 8 and 12 weeks

Evaluated using the visual analogue scale

次要结局

  • Changes on Ultrasound parameters(Baseline, after 4, 8 and 12 weeks)
  • Changes on quality of life(Baseline, after 4, 8 and 12 weeks)
  • Changes on function(Baseline, after 4, 8 and 12 weeks)

研究者

发起方
Federal University of São Paulo
申办方类型
Other
责任方
Principal Investigator
主要研究者

Jamille Godoy Mendes

MD

Federal University of São Paulo

研究点 (1)

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