跳至主要内容
临床试验/NCT02832713
NCT02832713Unknown2 期

Randomized Controlled Trial Comparing Botulin Toxin Versus Hyaluronic Acid by Intra-articular Injection for the Treatment of Painful Knee Osteoarthritis

University Hospital, Strasbourg, France1 个研究点 分布在 1 个国家目标入组 50 人开始时间: 2017年6月9日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
2 期
发起方
入组人数
50
试验地点
1
主要终点
Evaluation of pain measured using the WOMAC pain sub-score

研究概览

简要总结

In France, osteoarthritis affects about 10 million people and knee osteoarthritis represents 35% of cases. It is thought that more than 2.5 million people older than 65 years have knee osteoarthritis.

Currently, osteoarthritis management is based on three major axes:

  1. Non-pharmacological means, such as patient education, loss of weight and physical activity

  2. General pharmacological treatments: mainly paracetamol and then schedule II and III painkillers as well as nonsteroidal anti-inflammatory agent.

  3. Intra-articular pharmacological treatments:

  4. Intra-articular injections of corticosteroids: they are recommended during hydarthrotic flare-ups

  5. Intra-articular injections of hyaluronic acid (HA) (viscosupplementation) in the absence of intra-articular effusion. However, their efficacy is questioned by most experts in the case of symptomatic knee osteoarthrosis.

  6. Sometimes, surgery is the only therapeutic option. However, besides the fact of exposing patients, who are sometimes frail, to several peri- and post-operative complications, the recovery rate (variable according to the prosthesis type and ranging from 5% to 25% at 9 years) in an ageing population justifies waiting as much as possible before surgery. Therefore, it is important to test new therapeutic options for symptomatic osteoarthrosis that will allow postponing the surgical treatment.

  7. The use of botulinum toxin (BoNT-A) could thus represents an interesting alternative. BoNT-A is habitually used by intra-muscular injection for its myorelaxant effect in the management of painful reactive periarticular muscle contractures. However, BoNT-A has also antalgic activity independently of the myorelaxant effect. This allows explaining in part the antalgic effect of intra-articular BoNT-A injection. In the literature, six randomized controlled studies (RCS) have compared BoNT-A and intra-articular injections of corticosteroids, hyaluronic acid, or placebo. Only two RCS concerned knee osteoarthritis and compared BoNT-A to corticosteroids and a placebo, respectively, with a significant antalgic effect only in the groups treated with BoNT-A. No study has compared yet the intra-articular injection of BoNT-A to the viscosupplementation by HA in knee osteoarthritis and this is the aim of this trial.

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
Single (Outcomes Assessor)

入排标准

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

入选标准

  • Painful, or predominantly unilateral painful, knee osteoarthritis of any etiology
  • Knee without clinical signs of intra-articular effusion
  • Kellgren score ≥ II on X-ray
  • WOMAC pain sub-score ≥ 5 in the month preceding the inclusion visit

排除标准

  • Inflammatory arthropathy,infectious, neoplastic within the past year
  • Neuromuscular pathology
  • Cardiorespiratory pathology or any other severe disease that interferes with the functional capacities
  • Any decompensated or unstable chronic pathology
  • Glomerular filtration rate (GFR)<15 mL/min/1.73m²) within the past 6 months
  • HBA1c in diabetic people > 12% within the past 6 months
  • BMI ≥ 35kg/m2
  • Infection: joint, general, distant, cutaneous
  • Foreign material in the knee to be treated: prosthesis, osteosynthesis material
  • Severe coagulation problem: platelets <100000/mm3 within the past 6 months
  • Allergy to BoNT-A
  • Allergy to HA
  • Pregnant or breast-feeding women
  • Treatment with aminoglycosides or direct oral anticoagulants
  • Treatment with VKA (antihemorrhagic vitamin) if INR (International Normalized Ratio) higher than 3 within the past month
  • Change of anti-pain treatment less than 2 weeks before enrolment
  • Treatment with III pain killers or corticosteroids because of intense pain that does not respond to schedule I and II pain-killers
  • Intra-articular injection of corticosteroids in the previous two months
  • Viscosupplementation and/or injection of BoNT-A in the knee to be treated within the past 6 months
  • Injection of BoNT-A (except the knee to be treated) within the past 3 months
  • Swallowing troubles

研究组 & 干预措施

Intra-articular injection of botulinum toxin A

Experimental

干预措施: Botulinum toxin A ( BoNT-A) (Drug)

Intra-articular injection of hyaluronic acid

Active Comparator

干预措施: Hyaluronic acid (HA) (Device)

结局指标

主要结局

Evaluation of pain measured using the WOMAC pain sub-score

时间窗: Change from baseline WOMAC pain sub-score at 3 months

次要结局

  • Evaluation of the quality of life based on the SF-36 score(Before injection, 1 month, 3 months and 6 months following injection)
  • Frequency, seriousness and severity of adverse event reactions(during the 6 months following injection)
  • Changes in passive and active articular knee amplitude, by goniometry(Before injection, 1 month, 3 months and 6 months following injection)
  • Evaluation of the patients' functional improvement using the Timed Up-and-go Test(Before injection, 1 month, 3 months and 6 months following injection)
  • Evaluation of the patients' functional improvement based on the WOMAC score ("stiffness and function sub-score" and total score)(Before injection, 1 month, 3 months and 6 months following injection)
  • Evaluation of the antalgic effect of BoNT-A vs hyaluronic acid measured using a verbal rating scale (VRS)(1 week after injection)
  • Changes in muscular strenght et muscular trophicity (using dynanometer and measure of knee and thin circumference)(Before injection, 1 month, 3 months and 6 months following injection)
  • Changes in pain treatment score (using a correspondence table)(Change from baseline pain treatment score at 6 months)

研究者

发起方
University Hospital, Strasbourg, France
申办方类型
Other
责任方
Sponsor

研究点 (1)

Loading locations...

相似试验