跳至主要内容
临床试验/NCT04884880
NCT04884880Unknown不适用

Prospective, Multicentre, Randomized, Double-blind, Placebo-controlled Clinical Trial of Luo-Fu-Shan Plaster in the Treatment of Rheumatoid Arthritis

Guang'anmen Hospital of China Academy of Chinese Medical Sciences1 个研究点 分布在 1 个国家目标入组 180 人开始时间: 2021年5月14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
入组人数
180
试验地点
1
主要终点
The changes of Visual Analogue Scale(VAS) pain score

研究概览

简要总结

The aim of this study is to assess the efficacy and safety of Luo-Fu-Shan Plaster in patients with Rheumatoid Arthritis.

详细描述

The investigators are inspired by Chinese traditonal herb, an therapy for thousands of years, and take its advantage to make Luo-Fu-Shan Plaster in order to get an effective and safe treatment for active RA patients. The study is a multicenter, randomized, double-blind, placebo-controlled 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
Double (Participant, Investigator)

入排标准

年龄范围
18 Years 至 75 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Male or female subjects aged 18 to 75 years (time of get informed consent)
  • Documented diagnosis of rheumatoid arthritis, as defined by the American Rheumatism Association 1987 Revised Criteria.
  • Documented diagnosis of damp-heat syndrome according to Traditional Chinese Medicine.
  • If patients are receiving Disease-modifying anti-rheumatic drugs (DMARDs), then the doses should have been kept stable for at least 12 weeks.
  • If patients are receiving non-steroidal anti-inflammatory drugs (NSAIDs) or orally Chinese herbal medicine, then the doses should have been kept stable for at least 4 weeks.

排除标准

  • Skin allergies or broken skin;
  • Taking glucocorticoids,more than 10 mg daily.
  • Female patients who are pregnant, breast-feeding or planed to be pregnant;

研究组 & 干预措施

Luo-Fu-Shan Plaster 10g

Experimental

10g,once daily,4 weeks

干预措施: Luo-Fu-Shan Plaster (Drug)

Placebo

Placebo Comparator

10g,once daily,4 weeks

干预措施: The placebo 10g (Drug)

结局指标

主要结局

The changes of Visual Analogue Scale(VAS) pain score

时间窗: Day 1 to Week 4

The changes of Visual Analogue Scale(VAS) pain score of global health status, the patient's assessment of pain on a visual analogue scale. The score their pain intensity in the most affected joint on a 0-10 cm Visual Analogue Scale Score (VAS), ranging from no pain (0) to extremely pain (10).

次要结局

  • The changes of the Disease Activiyu Score (DAS28)(Day 1 to Week 4)

研究者

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

Quan Jiang

Director,Devision of Rhenumatology

Guang'anmen Hospital of China Academy of Chinese Medical Sciences

研究点 (1)

Loading locations...

相似试验