ISRCTN90251749已完成未知
The efficacy and safety of low-molecular-weight fucoidan in patients with atopic dermatitis: A randomized, double-blind, placebo-controlled trial
inkou Chang Gung Memorial Hospital0 个研究点目标入组 91 人开始时间: 2023年2月16日最近更新:
适应症
试验速览
- 阶段
- 未知
- 状态
- 已完成
- 发起方
- 入组人数
- 91
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
- 性别
- All
入选标准
- •1. Male and female patients between 4 and 60 years of age
- •2. Evidence of itchy skin (or parental report of scratching or rubbing), combined with three or more of the following:
- •2.1. History of involvement of the skin creases (e.g., fronts of the elbow, backs of knees, fronts of ankles, and areas around the neck or eyes)
- •2.2. History of asthma or hay fever
- •2.3. History of generally dry skin in the past year
- •2.4. Onset in a child under two years of age
- •2.5. Visible flexural dermatitis
- •3. SCORing Atopic Dermatitis (SCORAD) score greater than or equal to 16 points
- •4. Those who voluntarily agree to participate and sign the informed consent
排除标准
- •1. Other eczema disorders, such as contact dermatitis or seborrheic dermatitis, etc., assessed by a dermatologist
- •2. Other dermatological diseases related to skin pruritus, assessed by a dermatologist
- •3. Oral/injected steroids, leukotriene antagonists, immunosuppressants, systemic photochemotherapy, immunotherapy, allergen-specific immunotherapy, or Chinese herbal medicine within 1 month before enrollment
- •4. Unable to take the study medicine as scheduled or cooperate in filling out the questionnaire and taking a blood test
- •5. Allergy to fucoidan
- •6. Hyperthyroidism history
- •7. Suffering from serious infection requiring hospitalization(e.g., pneumonia, cellulitis, or sepsis) , assessed by a clinician
- •8. Severe dysfunctions of the organ (e.g., heart failure, liver failure, liver cirrhosis, or renal failure (eGFR <60 mL/min/1.73 m2)), assessed by a clinician
- •9. Women in pregnancy or in preparation for pregnancy, and those in lactation
研究者
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