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临床试验/CTRI/2016/03/006782
CTRI/2016/03/006782招募中未知

Efficacy and Tolerability of MetaDerm in Subjects withModerate to Severe Atopic Dermatitis - Nil

Haus Bioceuticals Inc0 个研究点目标入组 48 人开始时间: 待定最近更新:

试验速览

阶段
未知
状态
招募中
入组人数
48

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

  • Moderate to severe atopic dermatitis as determined by Physicianâ??s Global Assessment (PGA > 3.
  • Males and females, age 12 - 65 years old inclusive.

排除标准

  • Is currently participating or has participated in another interventional clinical study at this or any other facility in the past 2 weeks.
  • Currently or has been diagnosed or treated for cancer in the past 5 years.
  • Requires any topical or systemic medications that could affect the course of their atopic dermatitis during the study period (except inhaled steroids and/or stable antihistamines for asthma or allergies).
  • Has a known hypersensitivity to any corticosteroid creams.
  • Has any active infections or has used antibiotics in the past 7 days.
  • Has any physical attributes or skin conditions that might interfere with the clear visual or instrumental assessments.(i.e. cuts, sunburn, birth marks, tattoos, extensive scarring,excessive hair growth or acne).
  • Has an immunologic or infectious disease (e.g. hepatitis, tuberculosis, HIV or AIDS, lupus rheumatoid arthritis) which could place the subject at risk or interfere with the accuracy of the study results.
  • Has used any immunosuppressant drugs or immunotherapy within the past 30 days or 5 half-lives.
  • Is an employee of the sponsor company or clinical testing site.
  • Is dependent on oral medication for any skin disease/condition or could not, in the opinion of the Investigator tolerate the restriction of discontinuing the medicine as required in this study.
  • Is currently pregnant or lactating or planning to become pregnant in the next 6 months (using double contraception for prevention).
  • Has a history of keloid formation following skin injury.
  • Is routinely taking anti-coagulant medications (i.e. Plavix,Coumadin, warfarin, heparin, etc.)
  • Any other condition or factor the Investigator or their duly assigned representative believes may affect the ability of the subject to complete the study or the interpretation of the results.

研究者

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