跳至主要内容
临床试验/CTRI/2024/11/076965
CTRI/2024/11/076965尚未招募2/3 期

To evaluate the Nidan eEvum Samprapti of Sthaulya with special reference to Ashtadosha and its Upshyatmaka Parikshana by Vidangadi Churna

Government Ayurvedic P G College and Hospital Chaukaghat Varanasi1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2024年12月25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
Reduction in weight,improvement in ashtadosha symptoms and metabolic parameter changes.

研究概览

简要总结

Objective:To asses the effectiveness of Vidangadi Churna in treating Sthaulya with special reference to ashtadosha.

Participants:60 Adults diagnosed with Sthaulya meeting inclusion and exclusion criteria from OPD.

and IPD of department of Rog nidan Evum Vikriti Vigyana and Department of Kayachikitsa of Government PG Ayurvedic Medical College and Hospital Chaukaghat Varanasi.

Interventions: Vidangadi Churna: Administered according to a standardized protocol.

Primary outcome:Reduction in weight, improvement in Ashtadosha symptoms, and metabolic parameter changes.

Secondary outcome:Changes in digestive symptoms, quality of life, safety and tolerability, appetite regulation, and anthropometric measurements.

Follow up -15 Days

Time Period: 1 month

Data Analysis :Data will be analyzed using appropriate statistical methods to compare the

effectiveness of the interventions on the primary and secondary outcomes.

Ethical Considerations: The study will be conducted in accordance with ethical guidelines and with

informed consent from participants.

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
18.00 Year(s) 至 65.00 Year(s)(—)
性别
All

入选标准

  • 1- participants of both genders aged between 18 to 65 years.
  • 2- Body Mass Index (BMI) ≥ 30 kg/m², indicating overweight or obesity.
  • 3- Patient of Sthaulya presenting features as per Ayurvedic text.
  • 4- Presence of at least one of the Ashtadosha associated with Obesity.
  • 5- Willingness to participate in the study and provide informed consent.

排除标准

  • 1- Age below 18 years or above 65 years.
  • 2- BMI less than 30 kg/m².
  • 3- Unwillingness to participate in the study or provide informed consent.
  • 4- History of serious medical conditions (e.g., Cardiovascular disease, Renal failure, Hypothyroidism, Cushing’s Syndrome, Severe Anaemia, Uncontrolled Diabetes, Cancer and any other Chronic conditions).
  • 5- Pregnancy or breastfeeding.
  • 5- Use of medication or supplements that may interfere with the study outcomes.
  • (e.g. Steroid medications, Antidepressants and Contraceptive pills).

结局指标

主要结局

Reduction in weight,improvement in ashtadosha symptoms and metabolic parameter changes.

时间窗: 30 Days

次要结局

  • changes in digestive symptoms,quality of life,safety and tolerability,appetite regulation and anthropometric measurements.(45 Days.)

研究者

发起方
Government Ayurvedic P G College and Hospital Chaukaghat Varanasi
申办方类型
Government medical college
责任方
Principal Investigator
主要研究者

Dr Anandana

Government Ayurveda PG College and Hospital Chaukaghat, Varanasi, Uttar Pradesh 221002

研究点 (1)

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