CTRI/2020/04/024658尚未招募2 期
An open label Clinical trial to evaluate clinical efficacy and safety of Ayush AGT for external wounds.
试验速览
- 阶段
- 2 期
- 状态
- 尚未招募
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
- •.1 Patients of either sex with age between 18 and 60 years
- •2 Patients with Superficial externalwounds requiring dressing
- •3. Solitary wound not less than 1 inches (2.5 cm) in diameter
- •4 Patienwilling to participate in the study for 1 month
排除标准
- •1Known allergy/hypersensitivity to any of the components of the dressing
- •2.Wound associated with fracture
- •3.Wound associated with skin disorder that is chronic or currently active like psoriasis, eczema
- •4.Neurological deficit at wound site
- •5.Hemoglobin level <7.0 g/dl, serumalbumin <3 g/dl
- •6.Patients with concurrent Hepatic Dysfunction (defined as AST and/or ALT > 2 times of the upper normal limit) or Renal Dysfunction (defined as S.Creatinine > 1.2 mg/dl)
- •7.Known cases of Diabetes Mellitus, AIDS & other sexually
- •transmitted diseases, Malignancy or known history of coagulopathy
- •8.Patients receiving immune-suppressive medication
- •9.Pregnancy or lactation
- •10.Varicose veins/Deep Vein Thrombosis
- •11.Wounds requiring full thickness graft
- •12.Patients where a reference wound cannot be treated in isolation fromother wounds.
- •13.H/o hypersensitivity to any of thetrial drugs or their ingredients.
- •14.Patient taking participationin any other clinical trial
- •15.Any other condition which the Investigatorthinksmay jeopardize the study.
研究者
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