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临床试验/NCT05488067
NCT05488067招募中4 期

The Safety and Efficacy of Atorvastatin on Xanthoma in Alagille Syndrome

Children's Hospital of Fudan University1 个研究点 分布在 1 个国家目标入组 10 人开始时间: 2022年3月22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
招募中
入组人数
10
试验地点
1
主要终点
Grade change of xanthoma

研究概览

简要总结

To observe the efficacy and safety of atorvastatin on xanthoma in Alagille syndrome through a prospective study.

详细描述

Alagille syndrome (ALGS, OMIM 118450) is an important cause of chronic cholestasis in children, and the incidence rate is about 1:30000~1:50000. Most patients with ALGS have hypercholesterolemia. In severe cases, multiple xanthomas can be seen, and some patients are accompanied by severe itching and pain. Disfigured xanthomas affect the normal social interaction of patients, thereby causing physical and mental damage to children. At present, xanthoma caused by hypercholesterolemia can be cured by treating the primary disease, taking lipid-lowering drugs (such as bile acid chelators, ezetimibe, statins, etc.), or lipoprotein apheresis. If it affects the beauty or function, local treatment such as 33% trichloroacetic acid dot coating, carbon dioxide laser, liquid nitrogen freezing or surgical resection is feasible, and even surgical operation( such as portal vena cava anastomosis, liver transplantation). Compared with expensive lipoprotein apheresis and other invasive therapies, taking lipid-lowering drug has the advantages of higher acceptance, lower cost and higher safety. However, at present, there are no guidelines for application of oral lipid-lowering drugs in children under 6 years old with hypercholesterolemia. Therefore, the purpose of this study is to clarify the safety and efficacy of atorvastatin on xanthoma in ALGS , so as to provide reference for the treatment of ALGS patients' xanthomas.

Risk prevention and treatment: The patients began to take atorvastatin from a small dose, followed up closely in the early stage (2-4 weeks) to see if the patients had obvious discomfort such as myalgia, and monitored the changes of Biochemistry (CK, ALT, AST, etc.). If moderate or more serious adverse reactions occurred during the trial or the following laboratory abnormalities occurred (CK exceeded 10 times the upper limit of normal; ALT or AST had been continued to rise, exceeding 2 times the baseline value), atorvastatin was temporarily stopped, and patients should be rechecked within 2 weeks. It is necessary to reevaluate and decide whether to restart atorvastatin treatment.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

年龄范围
1 Day 至 17 Years(Child)
性别
All
接受健康志愿者

入选标准

  • Meet the ALGS diagnostic criteria;
  • Xanthoma of skin;
  • Before treatment with atorvastatin,non-HDL-C≥5.76mmol/L(223 mg/dL);
  • Informed consent;
  • Age 0-17 years old, male or female;
  • Taking bile acid chelator (colenemide) has no obvious effect or intolerance.

排除标准

  • Liver transplantation has been performed;
  • In the recovery period of cholestasis, xanthoma is obviously subsiding;
  • Patients with serious systemic diseases and unstable vital signs;
  • Progressive active liver injury, such as continuous increase of transaminase;
  • Serious myopathy;
  • Known to be allergic to any component of atorvastatin;
  • The weight is less than 5kg.

研究组 & 干预措施

Atorvastatin+ALGS-Xanthoma

Experimental

Drug: atorvastatin Dosage form: tablet Route of administration: oral Duration: 6 months (After 6 months of medication, according to the actual situation of the patient, choose to maintain the original dosage, gradually reduce the dosage or stop the medication)

Administration method:

Initial dose: ① < 1 year old: 1.25mg/d, qd; ② 1-5 years old: 2.5mg/d, qd; ③ 6-9 years old: 5mg/d, qd; ④ ≥ 10 years old: 10mg/d, qd. The maximum dose is 40mg/d and not more than 1mg/kg/d. During the follow-up, the medication was adjusted according to the laboratory results until non-HDL-C≤4.2mmol/L(162 mg/dL), xanthoma disappear, or the patient had moderate or more serious adverse reactions.

干预措施: atorvastatin (Drug)

结局指标

主要结局

Grade change of xanthoma

时间窗: from enrollment to the 3th/6th month

The grade change of xanthoma would be assessed at the 3th/6th month after enrollment 【Explanation:Xanthomas were graded as 0 = none, 1 = minimal, 2 =moderate, 3 = disfiguring, and 4 = disabling. Minimal xanthomas signified fewer than 20 scattered individual lesions, moderate represented more than 20 lesions that did not interfere with or limit activities, disfiguring represented large numbers of lesions that by their large numbers or size caused distortion of the face or xtremities, and disabling signified that the xanthomas interfered with function (such as hand use or ability to walk) because of excess size or number.】

次要结局

  • Incidence of adverse events(from enrollment to the 3th/6th month)
  • non-HDL-C change(from enrollment to the 3th/6th month)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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