跳至主要内容
临床试验/CTRI/2025/02/080705
CTRI/2025/02/080705尚未招募2/3 期

A Randomised Comparative Clinical Study to Determine the Effect of Kanakadi lepa with and without Siravyadha in Padadari.

Dr Amol Pawar1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2025年3月15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
60
试验地点
1
主要终点
Ruja (pain)

研究概览

简要总结

This is a single blind randomized comparative clinical study to evaluate the effect of kanakadi lepa with out without siravyadha in 15 days. This study comprise of two groups of 30 subjects with ruja ( pain), rukshata (dryness), daha ( burning sensation), kandu (itching) associated with  padadari. Study will be conducted in ALN Rao memorial ayurvedic hospitals in koppa , koppa taluk, chikmagaluru district 577126, karnataka, india. Primary out come measure will be ruja ( pain), rukshata (dryness), daha ( burning sensation), kandu (itching) in 15 days.

研究设计

研究类型
Interventional
分配方式
Randomized
盲法
Participant Blinded

入排标准

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

入选标准

  • 1.Age group.
  • 70yrs. 2.Subjects with fissures/ cracks in heel will be included irrespective of sex, economic status and religion. 3.Subjects with signs and symptoms of Padadari as mentioned in classical & contemporary texts such as ruja (pain), dari (cracks), kandu (itching), rukshata (dryness), daha (burning sensation). 4.The depth of the dari should be less than or equal to 1.5mm. 5.Subjects must be capable of giving consent, willingness and ability to comply with scheduled visits, treatment plans and laboratory tests and other study procedures.

排除标准

  • 1.Subjects with chronic systemic illnesses like uncontrolled Diabetes mellitus, hypertension, severe Anemia, Thalassemia, bleeding disorders, Cancerous conditions, HIV, HBsAg. 2.Conditions with infections, Cellulitis, Diabetic ulcers, Phlebitis, Liver diseases, Convulsive disorders, Paralysis, unconscious individual, pregnant woman.

结局指标

主要结局

Ruja (pain)

时间窗: 15 days

Rukshata (dryness)

时间窗: 15 days

Daha (burning sensation)

时间窗: 15 days

Kandu (itching)

时间窗: 15 days

次要结局

未报告次要终点

研究者

发起方
Dr Amol Pawar
申办方类型
Other [self]
责任方
Principal Investigator
主要研究者

Dr Amol Pawar

A L N Rao Memorial Ayurvedic Medical college and P.G. Center, Kopp

研究点 (1)

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