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临床试验/NCT06463379
NCT06463379招募中3 期

The Efficacy of Intravenous Pulse in Attaining Remission in Refractory Juvenile Idiopathic Arthritis

Sohag University1 个研究点 分布在 1 个国家目标入组 215 人开始时间: 2024年5月1日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
3 期
状态
招募中
入组人数
215
试验地点
1
主要终点
remission or low disease activity

研究概览

简要总结

Interventional phase 3 study aiming to unravel the value of pulse steroids in achieving remission or low disease activity in refractory active JIA

详细描述

First group will receive 2 consecutive days intravenous pulse of 125 mg methylprednisolone.

Second group will not receive additional drugs. Assessment was done at baseline and every month for 3 months for both groups using Juvenile Arthritis Disease Activity Score (JADAS) and the American College of Rheumatology Pediatric 30, 50, and 70 response criteria (ACR Pedi. 30, 50, 70).

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 (Participant)

入排标准

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

入选标准

  • Patients still active despite administration o 2 DMARDs

排除标准

  • Other connective tissue diseases
  • Endocrine disorders such as Thyroid disorders.

研究组 & 干预措施

pulse steroid

Experimental

108 patients will receive 125 mg solumedrol intravenous pulse for 2 consecutive days plus their concomitant medication.

干预措施: Solumedrol (Drug)

without pulse

Placebo Comparator

107 patients will not receive any additional medications.

干预措施: Solumedrol (Drug)

结局指标

主要结局

remission or low disease activity

时间窗: 3 months

patients will be assessed at baseline and every month for 3 months using Juvenile Arthritis Disease Activity Score (JADAS) for disease activity American College of Rheumatology Pediatric 30, 50, and 70 (ACR Pedi. 30, 50, 70) for disease activity

次要结局

未报告次要终点

研究者

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

Ahmed Mahrous

Professor

Sohag University

研究点 (1)

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