Controlled Clinical Trial to assess the effectiveness of topical application of C1 herbal oil on superficial external wounds and split thickness skin graft donor sites for surgical wound healing

Central Council for Research in Ayurvedic Sciences CCRAS0 个研究点目标入组 30 人开始时间: 待定最近更新: 2021年11月24日

试验速览

暂无简介。

•1. Known allergy/hypersensitivity to any of the components of the dressing
•2. Fracture/DVT of lower extremity
•3. A skin disorder that is chronic or currently active
•4. Polytrauma patients
•5. Wound at the surgical site prior to surgery
•6. Neurological deficit at wound site (Hemiplegia etc.)
•7. Haemoglobin level < 7.0 g/dl
•8. Serum Albumin <3 g/dl
•9. Subjects who, in the opinion of investigator, may not complete the study for any reason
•10. Hepatic failure, renal failure, coagulopathy, known cases of Diabetes mellitus
•11. Immunocompromised patients such as with Acquired immunodeficiency syndrome or receiving systemic immune suppression
•12. Patients who have psychiatric disorders or physical disabilities that hinders the study
•13. Pregnancy or Lactation
•14. Patient has history of poor wound healing, history of smoking/drug/alcohol abuse
•15. Poor prognosis patients unlikely to survive the trial period
•16. Patients where a reference wound cannot be treated in isolation from other wounds

发起方

Central Council for Research in Ayurvedic Sciences CCRAS