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临床试验/NCT02878018
NCT02878018Unknown不适用

Cohort Study on Traditional Chinese Medicine Diagnosis and Treatment of Children With Henoch-Schonlein Purpura Nephritis

Liaoning University of Traditional Chinese Medicine1 个研究点 分布在 1 个国家目标入组 600 人开始时间: 2016年9月最近更新:
适应症
干预措施

试验速览

阶段
不适用
发起方
入组人数
600
试验地点
1
主要终点
Urine erythrocyte

研究概览

简要总结

Henoch-Schonlein purpura nephritis(HSPN) is one of the most common secondary glomerulonephritis in children. A large, prospective, multicenter cohort study is being conducted in three institutions. Eligible Henoch-Schönlein purpura nephritis children will be classified as the experimental group (n=300) and the control group (n=300) based on the interventions they receive. Patients taking Chinese herbal formula will be in the experimental group, and those taking Western medicine will be in the control group. The entire study will last 60 weeks, including a 12-week observation period and a followup at 12 months.

详细描述

Background: Henoch-Schönlein purpura nephritis involves the renal impairment of Henoch-Schönlein purpura and can easily relapse into life-threatening late nephropathy in severe cases. Although there is a lack of validated evidence for its effectiveness, traditional Chinese medicine is the most commonly used method in China to treat Henoch-Schönlein purpura nephritis. We report the protocol of a prospective cohort trial using traditional Chinese medicine to investigate the effectiveness, safety and advantages for children with Henoch-Schönlein purpura nephritis.

Methods/Design: A large, prospective, multicenter cohort study is being conducted in three institutions. Eligible Henoch-Schönlein purpura nephritis children will be classified as the experimental group (n=300) and the control group (n=300) based on the interventions they receive. Patients taking Chinese herbal formula will be in the experimental group, and those taking Western medicine will be in the control group. The entire study will last 60 weeks, including a 12-week observation period and a followup at 12 months. Seven visits will be scheduled for each participant with visits in week 0, week 2, week 4, week 6, week 8, week 10 and week 12. The primary outcomes include the remission rate and the recurrence rate. The secondary outcomes include the urine erythrocyte effectiveness, the urine protein effectiveness, the hormone usage rate, the immunosuppressant usage rate, and the incidence rate of renal failure. Safety outcomes and any adverse reactions will be recorded during the study.

Discussion: This study will determine whether the Chinese herbal formula is helpful for treating Henoch-Schönlein purpura nephritis in children. The findings will provide a basis for further confirmatory studies.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

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

入选标准

  • 未提供

排除标准

  • 未提供

研究组 & 干预措施

TCM intervention

Participants with HSPN of the Heat-Toxin type will take the Qi-Ji Shen-Kang formula. HSPN patients of the Wet-Heat type will take the Zhu-Bai formula. Those of Qi-Deficiency with Blood-Stasis type will take the Yu-Shen formula.

干预措施: Qi-Ji Shen-Kang formula; Zhu-Bai formula; Yu-Shen formula (Drug)

WM conventional intervention

The WM conventional intervention, recommended by the Chinese Medical Association's (CMA) Scientific Statement, includes angiotensin-converting enzyme (ACE) inhibitor, adrenergic receptor binder (ARB), adrenal cortical hormone, Tripterygium wilfordii polyglycosidium and an immunosuppressant.

干预措施: angiotensin-converting enzyme (ACE) inhibitor; adrenergic receptor binder (ARB); adrenal cortical hormone; Tripterygium wilfordii polyglycosidium; immunosuppressant (Drug)

结局指标

主要结局

Urine erythrocyte

时间窗: 2 weeks

1. Recovery:Urine erythrocyte is normal. 2. Marked effect:Urine erythrocyte reduction is larger than 50%. 3. Effective:Urine erythrocyte reduction is smaller than 50%. 4. Ineffective;Urine erythrocyte has no changes.

Urine protein

时间窗: 2 weeks

1. Recovery:Urine protein(-). 2. Marked effect:Urine protein reduces by 2'+'. 3. Effective:Urine protein reduces by 1'+'. 4. Ineffective:Urine protein has no changes.

Creatinine clearance rate and Serum creatinine

时间窗: 1 year

Diagnostic criteria of chronic renal failure: 1. Creatinine clearance rate\<80ml/min; 2. Serum creatinine\>133μmol/L; 3. The patient who have a history of chronic kidney diseases or systemic diseases involving kidney.

24-hour urinary protein excretion

时间窗: 2 weeks

1. Recovery:24-hour urinary protein excretion is normal. 2. Marked effect:24-hour urinary protein excretion reduction is larger than 50%. 3. Effective:24-hour urinary protein excretion reduction is smaller than 50%. 4. Ineffective:24-hour urinary protein excretion has no changes.

次要结局

  • Number of patients with hormone therapy(3 months)
  • Number of patients with immunosuppressant therapy(3 months)

研究者

发起方
Liaoning University of Traditional Chinese Medicine
申办方类型
Other
责任方
Principal Investigator
主要研究者

Zhang Jun

Professor

Liaoning University of Traditional Chinese Medicine

研究点 (1)

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