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临床试验/NCT02951234
NCT02951234Unknown不适用

Kawasaki Disease Center, Kaohsiung Chang Gung Memorial Hospital, Taiwan

Chang Gung Memorial Hospital9 个研究点 分布在 1 个国家目标入组 278 人开始时间: 2016年9月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
发起方
入组人数
278
试验地点
9
主要终点
coronary artery lesions

研究概览

简要总结

Kawasaki disease (KD) is an acute febrile systemic vasculitis most commonly seen in children under the age of 5 years old. This trial has been designed as a multi-center, prospective, randomized controlled, evaluator-blinded trial with two parallel groups to determine whether IVIG alone as the primary therapy in acute-stage KD is as effective as IVIG combined with high-dose aspirin therapy. The primary endpoint is defined as CAL formation at 6-8 weeks.

详细描述

Background: Kawasaki disease (KD) is an acute febrile systemic vasculitis most commonly seen in children under the age of 5 years old. High-dose aspirin is often administered, but the duration of such treatment varies. Many centers reduce the aspirin dose once the patient is afebrile, even before treating said patient with IVIG. However, a randomized controlled trial regarding high-dose aspirin in the acute stage of KD has not previously been carried out.

Methods/design: This trial has been designed as a multi-center, prospective, randomized controlled, evaluator-blinded trial with two parallel groups to determine whether IVIG alone as the primary therapy in acute-stage KD is as effective as IVIG combined with high-dose aspirin therapy. The primary endpoint is defined as CAL formation at 6-8 weeks. Patients meeting the eligibility criteria are randomly assigned (1:1) to a test group (that receives only IVIG) or a standard group (that receives IVIG plus high-dose aspirin). This clinical trial is conducted at seven medical centers in Taiwan.

Discussion: Since high-dose aspirin has significant anti-inflammatory and anti-platelet functions, it does not appear to lower the frequency of disease outcomes. Furthermore, it can decrease hemoglobin levels. Therefore, the investigators have initiated this randomized controlled trial to determine whether high-dose aspirin is necessary in the acute stage of KD.

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
— 至 7 Years(Child)
性别
All
接受健康志愿者

入选标准

  • Male or female, under the age of 7 years old.
  • Fulfilled the AHA criteria for KD as explained below:
  • Fever (more than 38.0℃ ear temperature) > or = 5 days, as well as 4 of the 5 following symptoms
  • Diffuse mucosal inflammation (strawberry tongue, dry and cracked lips)
  • Bilateral non-purulent conjunctivitis
  • Dysmorphous skin rashes
  • Indurative edematous change over the hands and feet, or desquamation over the fingertips or toes
  • Cervical lymphadenopathy (one or more nodule at least 1.5 cm in diameter)
  • An informed consent form (ICF, appendix B) signed by the patient or a legal guardian.

排除标准

  • Had symptoms that did not completely match the KD criteria.
  • Had an acute fever for < 5 days and >10 days
  • IVIG treatment at another hospital before being referred to the study center.
  • Treatment with corticosteroids, other than the inhaled form, in the two weeks prior to joining the study;
  • The presence of a disease known to mimic Kawasaki disease (such as adenovirus infection, toxic shock syndrome etc.).
  • Previous KD diagnosis.
  • Inability to take aspirin (such as history of hypersensitivity to aspirin, G6PD deficiency, recent herpes zoster infection or vaccination, etc.)
  • Afebrile prior to enrollment
  • CAL prior to enrollment
  • Severe concomitant medical disorders (e.g., immunodeficiency, chromosomal anomalies, congenital heart diseases, metabolic diseases, nephritis, collagen diseases, etc.)
  • Suspected to have an infectious disease, including sepsis, septic meningitis, peritonitis, bacterial pneumonia, varicella, and influenza
  • Judged by the researcher to be unsuitable for this trial.

研究组 & 干预措施

IVIG only

Experimental

All patients will receive IVIG (2g/kg) in 10-12 hours alone, without high-dose aspirin. After fever subsides, low-dose aspirin (3-5mg/kg/day) will be prescribed until 6-8 weeks.

干预措施: IVIG only (Other)

IVIG and Aspirin

Active Comparator

All patients will receive IVIG (2g/kg) in 10-12 hours plus high-dose aspirin (80-100mg/kg/day, divided into four doses) till fever subside. After fever subsides, low-dose aspirin (3-5mg/kg/day) will be prescribed until 6-8 weeks.

干预措施: IVIG and Aspirin (Other)

结局指标

主要结局

coronary artery lesions

时间窗: 8 weeks

次要结局

  • IVIG resistance(7 days)

研究者

发起方
Chang Gung Memorial Hospital
申办方类型
Other
责任方
Sponsor

研究点 (9)

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