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临床试验/NCT03411798
NCT03411798已完成4 期

Sequential Application of Yisaipu® and Disease Modifying Anti-Rheumatic Drugs (DMARDs) in Treating Mild-to-Moderate Ankylosing Spondylitis: the Mid-term Follow-up Result

Nanfang Hospital, Southern Medical University1 个研究点 分布在 1 个国家目标入组 76 人开始时间: 2017年12月15日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
4 期
状态
已完成
入组人数
76
试验地点
1
主要终点
ASAS 20

研究概览

简要总结

The drug regimes in treating ankylosing spondylitis(AS) have limitations. The tumor necrosis factor inhibitors(TNFi) was effective but expensive. Disease modifying anti-rheumatic drugs (DMARDs) were cheap but insufficient. This study proposed a sequential usage of TNFi, the Yisaipu®, and DMARDs, and aims to evaluate the mid-term therapeutic effect of this new scheme in treating the mild-to-moderate AS.

研究设计

研究类型
Interventional
干预模型
Sequential
主要目的
Treatment
盲法
None

入排标准

性别
All
接受健康志愿者

入选标准

  • 1.Clinical diagnosis of Ankylosing Spondylitis(AS) based on modified New York diagnostic criteria for AS (1984) 2.At the mild-to-moderate stage of AS disease 3.At the active phase of AS disease

排除标准

  • 1.Active tuberculosis, hepatitis, tumors, infection diseases or combine with other rheumaimmune systemic diseases or osteoarthritis diseases 2.Pregnant or breastfeeding women

研究组 & 干预措施

Experimental

Experimental

Yisaipu® was introduced only during the active state and was switched to DMARDs, methotrexate(MTX), sulfasalazine(SSZ) and hydroxychloroquine(HCQ), after disease remission (ESR & CRP reduce to normal and BASDAI<4) maintenance.

干预措施: Yisaipu® (Drug)

结局指标

主要结局

ASAS 20

时间窗: 12 months after

Improvement of \>20% and \>1 unit in at least 3 domains on a scale of 10;No worsening of \>20% and \>1 unit in remaining domain on a scale of 10 compare to the baseline status

ASAS 40

时间窗: 12 months after

Improvement of \>40% and \>2 unit in at least 3 domains on a scale of 10;No worsening at all in remaining domain compare to the baseline status

次要结局

  • BASDAI(baseline,3 months after,6 months after,12 months after)
  • Patient Global Assessment(baseline,3 months after,6 months after,12 months after)
  • CRP(baseline,3 months after,6 months after,12 months after)
  • ESR(baseline,3 months after,6 months after,12 months after)
  • BASFI(baseline,3 months after,6 months after,12 months after)
  • SQOL-AS(baseline,3 months after,6 months after,12 months after)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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