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临床试验/NCT05527964
NCT05527964已完成不适用

The Influence of Specific Targeted Therapy on Subject and Family Quality of Life, Anxiety, Depression and Sleep Quality in Patients With Severe Refractory Atopic Dermatitis in the Czech Republic

Sanofi1 个研究点 分布在 1 个国家目标入组 146 人开始时间: 2022年12月30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
Sanofi
入组人数
146
试验地点
1
主要终点
The regression coefficient for at least 75% reduction in the Eczema Area and Severity Index score (EASI75) at week 24 adjusted to baseline characteristics predicting the change in EQ-5D utility

研究概览

简要总结

Assessment of the relationship between treatment response (EASI75) and change in quality of life (EQ-5D) by week 24.

Description of the:

  • Change in disease activity after 16 and 24 weeks
  • Change in subject and family quality of life after 16 and 24 weeks
  • Change in sleep quality after 16 and 24 weeks
  • Change in anxiety after 16 and 24 weeks
  • Change in depression after 16 and 24 weeks
  • Safety and tolerability

详细描述

28 weeks

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Patient eligible for Dupixent therapy of AD according to the current SPC and reimbursement criteria given by the SUKL
  • Signed informed consent
  • 18 years and older (study questionnaires are validated for this age group). Patient is able to follow the prescribed regimen, routine follow-up visits and to fill the questionnaires

排除标准

  • Patient not eligible for Dupixent therapy of AD according to the current SPC and reimbursement criteria given by the SUKL.
  • The above information is not intended to contain all considerations relevant to a potential participation in a clinical trial.

结局指标

主要结局

The regression coefficient for at least 75% reduction in the Eczema Area and Severity Index score (EASI75) at week 24 adjusted to baseline characteristics predicting the change in EQ-5D utility

时间窗: At Week 24

次要结局

  • Total number of adverse events(At Week 16 and Week 24)
  • Change in anxiety (Clinically Useful Anxiety Outcome Scale (CUXOS) score)(At Week 16 and Week 24)
  • Change in disease activity (Eczema Area and Severity Index (EASI) score)(At Week 16 and Week 24)
  • Reasons for discontinuations(At Week 16 and Week 24)
  • Change in subject generic quality of life (European Quality of Life Five Dimension questionnaire (EQ-5D) utility)(At Week 16 and Week 24)
  • Change in Family Dermatology Life Quality Index (FDLQI score)(At Week 16)
  • Change in sleep quality (Jenkins Sleep Evaluation Questionnaire (JSEQ) score)(At Week 16 and Week 24)
  • Total number of discontinuations(At Week 16 and Week 24)
  • Change in Dermatology Life Quality Index (DLQI score)(At Week 16 and Week 24)
  • Change in depression (Clinically Useful Depression Outcome Scale (CUDOS) score)(At Week 16 and Week 24)
  • Number of non-serious adverse events (non-SAEs)(At Week 16 and Week 24)
  • Number of serious adverse events (SAEs)(At Week 16 and Week 24)

研究者

发起方
Sanofi
申办方类型
Industry
责任方
Sponsor

研究点 (1)

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