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临床试验/TCTR20220413003
TCTR20220413003已完成4 期

A COMPARISON OF THE EFFICACY OF STEROID PATCH CONTAINING BETAMETHASONE17 ,21DIPROPIONATE TO TOPICAL BETAMETHASONE17 ,21DIPROPIONATE TO TREAT IN CHRONIC HAND ECZEMA

Faculty of Medicine, Srinakharinwirot University0 个研究点目标入组 56 人开始时间: 2022年4月13日最近更新:
适应症

试验速览

阶段
4 期
状态
已完成
发起方
入组人数
56

研究概览

简要总结

The transdermal corticosteroid patch group demonstrated its safety and effectiveness, showing comparability to topical corticosteroids after 8 weeks of application. The patch's sustained-release features, when combined with once-daily application, have potential to enhance patient satisfaction and encourage better treatment adherence.

研究设计

研究类型
Interventional

入排标准

年龄范围
18 Years 至 N/A (No limit)(—)
性别
All

入选标准

  • 1. Female or male patients aged over 18 years old.
  • 2. Patients who have been diagnosed as mild to moderate chronic hand
  • eczema or have history of intermittent or persistent skin lesions such as eczematous or
  • vesicles on both hands for more than 3 consecutive months or relapse more than twice
  • a year with or without prior treatment.
  • 3. Patients who have been assessed HECSI score as 0-27 and defined as
  • mild to moderate severity.
  • 4. Patients who participate in the project voluntarily and sign the consent
  • 5. Patients who are able to follow-up examination in the 2nd, 4th, and 8th

排除标准

  • 1. Patients who have current or active bacterial, fungal, or viral infection of
  • 2. Patients who allergic to component of ingredients in topical steroid
  • ointment or patch using in this study as shown in Table 7 and 8.
  • 3. Female patients who are pregnant, lactating or planning to become
  • pregnant during the study period.
  • 4. Patients who have history of treatment with topical corticosteroids or
  • topical calcineurin inhibitors within 2 weeks before and during this study.
  • 5.Patients who have history of treatment with systemic corticosteroids,
  • immunosuppressant such as cyclosporin, azathioprine, mycophenolate mofetil, and
  • phototherapy within 4 weeks before and during this study

研究者

发起方
Faculty of Medicine, Srinakharinwirot University

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