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临床试验/CTRI/2020/11/029074
CTRI/2020/11/029074尚未招募未知

Methotrexate and Prednisolone study in Erythema Nodosum Leprosum - MaPs in E

ondon School of Hygiene and Tropical Medicine0 个研究点目标入组 0 人开始时间: 待定最近更新:

试验速览

阶段
未知
状态
尚未招募
发起方

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

  • All of the following six criteria must be met in order for an individual to be eligible (only one of 6A to 6D need to be met):
  • 1. Individuals who diagnosed with leprosy complicated by ENL
  • 2. Individuals with ENL aged 18-60 years old
  • 3. Individuals with ENL deteriorating symptoms
  • 4. Individuals with 10 or more tender, papular or nodular ENL skin lesions
  • 5. Individuals with an EESS score of at least 9
  • 6. Individuals with ENL on:
  • A. No current anti- ENL treatment
  • B. Prednisolone up to 30mg per day (if ACUTE) or Prednisolone 10-30mg (inclusive) per day (if RECURRENT/ CHRONIC) or equivalent alternative corticosteroid dose OR
  • C. Thalidomide or other non-steroidal anti-ENL medication OR
  • D. A combination of prednisolone (up to 30mg) and another non-steroidal anti-ENL medication (thalidomide, clofazimine, azathioprine, pentoxifylline, ciclosporin, minocycline)

排除标准

  • 1) Individuals who were first diagnosed with ENL more than 4 years prior to enrolment
  • 2) Individuals less than 18 years old or older than 60 years
  • 3) Individuals weighing less than 35kg
  • 4) Individuals with 9 or fewer tender, popular or nodular ENL skin lesions
  • 5) Individuals with an EESS score of 8 or less
  • 6) Women of child bearing capacity who decline to use two forms of adequate contraception and men who decline to use two forms of adequate contraception
  • 7) Pregnant or breastfeeding women
  • 8) Individuals with recurrent or chronic ENL who deteriorate on a dose of prednisolone less than 10 mg or more than 30 mg
  • 9)Individuals who have taken methotrexate by any route for the last 12 weeks
  • 10)Individuals with a hypersensitivity to methotrexate or a recognised contraindication ( please see Methotrexate information sheet)
  • 11) Individuals currently diagnosed with Type 1 reaction or Lucioâ??s phenomenon
  • 12) Individuals with the severe abnormalities in screening investigations
  • 13) Positive serology for HIV, Hepatitis B or C
  • 14) Evidence of tuberculosis or pulmonary fibrosis
  • 15) A history of chronic liver disease or excessive alcohol or illicit substance consumption
  • 16) Individuals with severe inter-current infections, uncontrolled diabetes, active peptic ulcer disease, untreated malignancy
  • 17) Individuals unable to attend regularly for assessment or monitoring

研究者

发起方
ondon School of Hygiene and Tropical Medicine

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