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临床试验/CTRI/2024/11/076833
CTRI/2024/11/076833尚未招募2 期

A Comparative Pharmaceutical And Clinical Study Of Kandughna Mahakashaya Vati And Taila And Their Effect On Vicharchika With Special Reference To Eczema

Government PG Ayurvedic College And Hospital1 个研究点 分布在 1 个国家目标入组 90 人开始时间: 2024年11月30日最近更新:

试验速览

阶段
2 期
状态
尚未招募
发起方
入组人数
90
试验地点
1
主要终点
Improvement in Eczematous Lesions and Itching

研究概览

简要总结

This study is interventional study trial comparing the efficacy of Kandughna mahakashaya in two different dosage form. patients will be randomly be selected from OPD of department of Rasa Shastra And Bhaishajya Kalpana and Swasthavritta, at government P.G ayurvedic college and hospital , varanasi.

90 patients will be studied under 3 group having 30 patients in each group.

Group A- 30 Patients will be treated by Kandughna mahakashaya Vati for 28 days.

Group B- 30 Patients will be treated by Kandughna mahakashaya Taila for 28 days.

Group C- 30 Patients will be treated by Kandughna mahakashaya Vati and Taila for 28 days.

Follow up will be done after every 07 days of treatment in each group.

Total duration of treatment plan is 28 days.

研究设计

研究类型
Interventional
分配方式
Other
盲法
None

入排标准

年龄范围
16.00 Year(s) 至 60.00 Year(s)(—)
性别
All

入选标准

  • Patients presenting with sign and symptoms of Vicharchika (Eczema) like Kandu (Itching), Pidika (Papules), Shyava (Blackish discolouration), Srava (Oozing), Rajyo (Disintegrity of skin), Ruja (Pain), Rukshta (Dryness) are selected for study.
  • Patients having history with of one month or less than one months of origin of Vicharchika (Eczema).

排除标准

  • Patients having age group of less than 16 years and above 60 years.
  • Patients with any systemic disorders like uncontrolled hypertension, diabetes mellitus, hypothyroidism/hyperthyroidism and Pregnant & Lactating women.
  • Patients who are using corticosteroid since long term.
  • Patients of status Eczematous condition.
  • Patients of Vicharchika (Eczema) having other skin disorder.

结局指标

主要结局

Improvement in Eczematous Lesions and Itching

时间窗: 7 Days,14 Days,21 Days

次要结局

  • Complete Relief In Eczematous Lesions And Itching(28 Days)

研究者

发起方
Government PG Ayurvedic College And Hospital
申办方类型
Research institution and hospital
责任方
Principal Investigator
主要研究者

Dr Sandeep Kumar

Government P.G Ayurvedic College And Hospital

研究点 (1)

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