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临床试验/ISRCTN12758639
ISRCTN12758639已完成不适用

Reduction of adverse effects by systemic antihistamines during therapy with fumarates in severe chronic plaque psoriasis

Erasmus Medical Center (The Netherlands)0 个研究点目标入组 40 人开始时间: 2006年11月22日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
40

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

入选标准

  • 1. Patients with known severe psoriasis of the chronic plaque type
  • 2. Psoriasis Area and Severity Index (PASI) more than ten
  • 3. Age more than 18 years
  • 4. Psoriasis therapies cannot be administered starting from 28 days before baseline visit until discontinuation of the study medications at the end of the study
  • 5. All forms of ultraviolet light therapy are prohibited during the study through week 12, such as Psoralen Ultraviolet A therapy (PUVA) and Ultraviolet B (UVB) (including narrow band UVB and excimer laser). PUVA is prohibited starting from 28 days before the baseline and UVB is prohibited starting from 14 days before baseline
  • 6. All forms of topical psoriasis therapies cannot be administered from 14 days before baseline until discontinuation of the study medications through week 12
  • 7. Investigational or biological drugs are not permitted from 28 days prior to screening visit until discontinuation of the study medication at the end of study

排除标准

  • 1. Pregnancy and breast-feeding
  • 2. Patients with prostate hyperplasia, glaucoma, stomach ulcer
  • 3. Patients with liver diseases
  • 4. Patients with kidney diseases
  • 5. Patients with blood test deviations
  • 6. Patients with gastro-intestinal diseases
  • 7. Patients with a history of malignancies
  • 8. Presence of clinically significant renal and hepatic laboratory values (i.e., male patients with serum creatinine more than or equal to 133 umol/L; female patients with serum creatinine more than or equal to 124 umol/L; Alanine Aminotransferase [ALT], Aspartate Aminotransferase [AST], total bilirubin, Gamma-Glutamyl Transferase [GGT], or Alkaline Phosphatase more than 2.5 times the upper limit of the reference range)
  • 9. Serum lipase impairments (total cholesterol more than 6.5 mmol/l, Low Density Lipoprotein [LDL]-cholesterol less than 2 mmol/l, triglyceride more than 3 mmol/l).
  • 10. Haemoglobin parameters must satisfy the following criteria:
  • a. haemoglobin less than 7.5 mmol/l
  • b. leukocytes more than 3.50 x 10^9/l and less than 10 x 10^9/l
  • c. lymphocytes more than 15% and less than 50% of the total white cell count

研究者

发起方
Erasmus Medical Center (The Netherlands)

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