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临床试验/CTRI/2020/04/024658
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.

Central council for Research in Ayurvedic Sciences0 个研究点目标入组 0 人开始时间: 待定最近更新:

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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