跳至主要内容
临床试验/CTRI/2024/10/074895
CTRI/2024/10/074895尚未招募2/3 期

Randomised controlled clinical trial to compare the efficacy of external use of Panchavalkala siddha ghrita with betadine ointment in the management of vidradhi Bhedan pashchat vrana.

Tilak Ayurveda Mahavidyalaya1 个研究点 分布在 1 个国家目标入组 74 人开始时间: 2024年10月23日最近更新:

试验速览

阶段
2/3 期
状态
尚未招募
发起方
入组人数
74
试验地点
1
主要终点
Decrease in size, pain, vranoshtha, redness.

研究概览

简要总结

The study will be intervened by the treatment of Panchvalkala siddha Ghrita and Betadine ointment to group A and group B respectively. The efficacy of the therapy will be assessed on the basis of subjective criteria for statistical analysis. Scoring will be designed according to the severity of symptoms. The subjective gradation of symptoms will be done as follows and the intensity of each symptom will be calculated before treatment, after treatment and after follow up. The effect of treatment result will be assessed in regards to clinical signs and symptoms on the basis of grading and scoring system. The signs and symptoms will be assessed by adopting the suitable scoring method.

研究设计

研究类型
Interventional
分配方式
Coin toss, Lottery, toss of dice, shuffling cards etc
盲法
None

入排标准

年龄范围
20.00 Year(s) 至 70.00 Year(s)(—)
性别
All

入选标准

  • Patients with minor (dimensions, length: 1cm-6cm, depth: up to 1cm) and clean freshuninfected wound irrespective of age, sex, religion and socioeconomic class.
  • Post op incised & drained wound.

排除标准

  • HBsAg and HIV positive subjects, D.M., Tuberculosis and Leprosy patients.
  • Cases of orthopedic operatives, MRM, etc.
  • and other major surgeries.
  • More than 6cm size of wound.

结局指标

主要结局

Decrease in size, pain, vranoshtha, redness.

时间窗: 7days

次要结局

  • Decrease in size, pain, vranoshtha, redness, granulation tissue and tenderness(15 days)

研究者

发起方
Tilak Ayurveda Mahavidyalaya
申办方类型
Private medical college
责任方
Principal Investigator
主要研究者

Buddhiraj Satish Tupare

Tilak Ayurved Mahavidyalaya

研究点 (1)

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