CTRI/2009/091/000039已完成3 期
RANDOMIZED OPEN-LABEL COMPARATIVE MULTI-CENTRE TRIAL FOR EVALUATION OF EFFICACY, SAFETY AND TOLERABILITY OF HALOMETASONE 0.05% W/W & FUSIDIC ACID 2% TOPICAL CREAM VERSUS BETAMETHASONE VALERATE 0.12% W/W & NEOMYCIN SULPHATE 0.5% W/W TOPICAL CREAM IN THE TREATMENT OFACUTE OR CHRONIC INFECTED ECZEMATOUS DERMATOSIS
试验速览
- 阶段
- 3 期
- 状态
- 已完成
- 入组人数
- 150
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
- •Adults male and females with infected eczematous dermatosis aged > 18 years
排除标准
- •History of hypersensitivity to any of the drugs or stated excipients
- •Unwilling to give written informed consent
- •Uncontrolled Diabetes mellitus
- •Recent tubercular, syphilitic or viral skin infections
- •Concomitant diseases ?Leukemia, Parasitic diseases (i.e.Scabies, Pediculosis) or hypogammaglobulinemia
- •Patient in need of any form of treatment which influences the healing of the lesion such as topical treatment other than trial preparation, topical radiation therapy, systemic medication with antibiotics, antimicrobials, antihistaminic, cytostatics, corticosteroids or ACTH.
- •Pregnant and nursing women
- •Patients with clinically significant cardiovascular, hematological, pancreatic, metabolic, neurological or clinically significant laboratory abnormalities, which in the judgement of the investigator, would interfere with, subject participation in the study or evaluation of subject?s response to therapy.
- •Inclusion of the subject more than once in this trial is not allowed.
- •Participation in any other clinical trial involving investigational products within 30 days of screening.
研究者
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