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临床试验/NCT01927484
NCT01927484终止不适用

Methotrexate in Hand Osteoarthritis

University of Alexandria1 个研究点 分布在 1 个国家目标入组 2 人开始时间: 2020年3月7日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
终止
入组人数
2
试验地点
1
主要终点
pain reduction

研究概览

简要总结

Osteoarthritis (OA) is a common disabling condition, for which no effective therapy currently exists. Synovitis has been demonstrated in hand OA imaging. Synovial inflammation due to the release of cytokines is an important cause of pain. Methotrexate (MTX) helps to decrease synovitis in many inflammatory joint diseases, particularly rheumatoid arthritis.

The aim of the present study is to assess the efficacy of MTX in decreasing pain and inflammation in symptomatic hand OA.

Methods: One hundred and twenty patients with American College of Rheumatology (ACR) clinical and radiographic criteria of primary knee OA with hand pain, [>4 on the 24-hour average pain severity scale (0-10) using mean of daily ratings from week preceding randomization] for > 14 days/month during 3 consecutive months preceding enrollment will be included in this randomized double-blind placebo-controlled trial. Patients meeting the eligibility criteria were randomized in a 1:1 ratio to receive either 25mg/week oral MTX (n=60) or placebo (n=60) together with their usual therapy provided the dosages were kept constant for 28 weeks. Pain will be assessed using the Visual Analogue pain Scale, (VAS, 0-100 mm). Functional assessment will be performed using the Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC) and Activities of daily living (ADL) scores. Alterations in dosage of analgesic/NSAID drugs used will be recorded. Safety and tolerability will also be assessed. Synovitis will be detected by ultrasound imaging.

研究设计

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

入排标准

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

入选标准

  • primary knee osteoarthritis
  • persistent pain
  • synovitis

排除标准

  • rheumatoid arthritis
  • gout and pseudogout
  • traumatic arthritis
  • other secondary arthritis
  • renal disease
  • liver disease

研究组 & 干预措施

methotrexate

Experimental

25mg oral methotrexate tablets

干预措施: 25 mg/week oral methotrexate tablets (Drug)

placebo

Placebo Comparator

25 mg/week placebo tablets

干预措施: 25mg/week oral placebo tablets (Drug)

结局指标

主要结局

pain reduction

时间窗: 28 weeks

The primary outcome will be pain reduction at 28 weeks compared to baseline using a Visual Analogue Pain Scale (VAS) 0-100 mm. Data will be collected at baseline and monthly up to 28 weeks to determine any change in results from those obtained at baseline.

次要结局

  • physical function improvement Functional assessment(28 weeks)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Anna Abou-Raya

MD

University of Alexandria

研究点 (1)

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