跳至主要内容
临床试验/CTRI/2020/07/026422
CTRI/2020/07/026422尚未招募2 期

A Randomized, Open Labeled, Clinical Study to evaluate the effect of Yashad-Jatyadi Ointment in Dushtavrana With Special Reference to Diabetic Foot Ulcer.

DrRamesh B Jadhav0 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
发起方

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 in the age group of 21 to 70 years (both inclusive).
  • 2)Patients having either Type I or Type II diabetes with non-healing diabetic foot ulcers.
  • 3)Diabetic patients having HbA1C <8.
  • 4)Patients having either Diabetic foot ulcers with the following ulcer characteristics :
  • a)Neuropathic and mild Neuro-ischaemic diabetic foot ulcer (single or multiple ulcers)
  • b)Diabetic foot ulcers with Grade 1 to 2 (Wagenerâ??s classification)
  • c)Duration of ulcer more than 1 month
  • d)Surface area of the Non-Healing Ulcer more than 1 cm2.

排除标准

  • 1)Patients with ischemic Ulcers (Diagnosed Clinically and /OR with Doppler)
  • 2)Known cases of Severe/Chronic Hepatic or Renal disease
  • 3)Known cases of any active malignancy.
  • 4)Patients giving history of significant cardiovascular event < 12 weeks prior to randomization.
  • 5)Chronic alcoholics / Alcohol abuse
  • 6)Patients ECG demonstrating any signs of uncontrolled arrhythmia / acute ischemia.
  • 7)Patients X-ray chest showing any active lesion of tuberculosis.
  • 8)Patients having known chronic, contagious infectious disease, such as active tuberculosis Hepatitis B or C, or HIV.
  • 9)Patients using any other investigational drug within 1 month prior to recruitment.
  • 10)Known hypersensitivity to any of the ingredients used in study drug.
  • 11)Pregnant and lactating females.
  • 12)Patients currently participating in any other clinical study or any education treatment program for Ulcers.
  • 13)Patients having any other medical or surgical condition considered unsuitable for his/her participation in the study as per investigatorâ??s judgment.
  • 14)Patients receiving drugs, which may interact with the study therapeutic protocol such as glucocorticoids, immunosuppressive and cytotoxic drugs.
  • 15)Patients who have undergone ulcer treatments with cell therapy, dermal substitutes, or other biological therapies within the last 30 days.

研究者

发起方
DrRamesh B Jadhav

相似试验