CTRI/2015/12/006443进行中（未招募）4 期
A randomized controlled trial of topical Mupirocin versus Mupirocin with Sucralfate combination in chronic skin ulcers.
Strassenburg Pharmaceuticals Ltd0 个研究点目标入组 90 人开始时间: 待定最近更新:
试验速览
- 阶段
- 4 期
- 状态
- 进行中（未招募）
- 发起方
- 入组人数
- 90
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
- •Patients of either sex of age > 18 years
- •Patients having grade 1 and grade 2 ulcer according to Wagner grading system.
- •Ulcer of duration > 4 weeks.
- •Wagner grading system
- •AGrade 1Superficial ulcer
- •BGrade 2Ulcer extension
- •1. Involves ligament, tendon, joint capsule or fascia
- •2. No abscess or osteomyelitis
- •CGrade 3Deep ulcer with abscess or osteomyelitis
- •DGrade 4Gangrene
- •EGrade 5Extensive gangrene
排除标准
- •Female patients who are pregnant or breast-feeding.
- •Patients having ulcer grade >2 according to Wagner grading system
- •Ulcer of duration > 6 months.Patients diagnosed to have decubitus ulcer.
- •Patients diagnosed to have ulceration due to malignancy.
- •Patients who have used formulations containing mupirocin or sucralfate for their ulcer within the last 4 weeks.
- •Patients with history of hypersensitivity to formulations containing mupirocin or sucralfate.
- •Patients suffering from debilitating chronic diseases including frankly uncontrolled diabetes and advanced malignancy.
- •Patients suffering from frankly immunocompromising disorders such as HIV/AIDS.
- •Patients on systemic antimicrobials, corticosteroids or any other medication known to influence wound healing currently or within last 4 weeks.
- •Patients suffering from alcoholism, substance abuse or psychiatric disorders that are liable to make them unreliable trial subjects.
- •Patients without adequate caregiver support at home who can supervise application of medication.
- •Any other condition which, in the opinion of the investigators, is likely to substantially increase the risk of non-adherence or the possibility of confounding of results.
研究者
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