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临床试验/CTRI/2025/12/098982
CTRI/2025/12/098982尚未招募2 期

A Randomized Clinical Study On Krimighanadi Kashaya In Sthoulya With Special Reference To Obesity

Jammu Institute Of Ayurveda And Research1 个研究点 分布在 1 个国家目标入组 30 人开始时间: 2026年5月1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
30
试验地点
1
主要终点
Improvement in Subjective and objective Parameters of Sthoulya

研究概览

简要总结

This clinical study aims to evaluate the efficacy of Krimighanadi Kashaya in the management of Sthoulya (Obesity), a condition described in Ayurveda as Medo-dhatu vriddhi associated with Kapha-Vata imbalance and classified under Ashtau Nindita. With the global rise of obesity and its related metabolic complications, there is a growing need for safe, sustainable, and holistic treatment approaches. Ayurveda offers a comprehensive management strategy through Nidana-parivarjana, Ahara-Vihara regulation, and Medohara therapies. Krimighanadi Kashaya, a classical formulation containing Vidanga, Triphala, Ajmoda, Katuki, Trikatu, Guggulu, and Amrita, is traditionally indicated for Kapha-Medo disorders due to its Deepana-Pachana, Lekhana, Agnivardhaka and Medohara actions. This single-arm, open-label, randomized pre-post clinical trial will include 30 participants aged 18–60 years with BMI 25–39.9 kg/m². The intervention will be administered for 30 days with follow-ups on days 15, 30, and 45, assessing both Ayurvedic and biomedical parameters such as subjective symptoms of Sthoulya and BMI. The study intends to generate evidence on the therapeutic potential, safety, and overall effectiveness of Krimighanadi Kashaya in improving obesity-related clinical outcomes and restoring metabolic balance.

研究设计

研究类型
Interventional
分配方式
Randomized
盲法
None

入排标准

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

入选标准

  • 1.Patients of either sex of age between 18years to 60 years.
  • 2.Patients having signs and symptoms of Obesity like large body frame having extra fat around the waist, difficulty in doing daily activities, lethargy, breathlessness increased weight, snoring, having sweating difficulty while sleeping.
  • 3.Patients having classical signs and symptoms of Sthoulya like Chal Udara Stana Sphika, Javoparodha, Kruchvyavaya, Dourbalyta , Atikshudha, Atitrishna etc.
  • 4.Patients with BMI between 25kg/m2 to 39 kg/m2 5.Patients willing to participate and able to provide signed informed consent.

排除标准

  • 1.Patients age less than 18 and more than 60 years.
  • 2.Pathophysiology or Genetic Syndromes associated with Sthoulya.
  • 3.Malignancy, poorly controlled diabetes mellitus, hypertension.
  • 4.Patients suffering from pulmonary diseases, cardiac diseases will not be taken from study.
  • 5.Alcoholic and drug abusers, pregnant and lactating women.

结局指标

主要结局

Improvement in Subjective and objective Parameters of Sthoulya

时间窗: Assessment: Percentage relief in symptoms and signs after 30 days of treatment.

Subjective:. Dourgandya

时间窗: Assessment: Percentage relief in symptoms and signs after 30 days of treatment.

Ang Gourava,Utsaha Hani,Kshudra Swasa,Ati Pipasa, Chala Spikha Udara Stana,Dourbalya,Nidraadhikya,Swedadhikya Snigdhangata,Alpa Vyavaya

时间窗: Assessment: Percentage relief in symptoms and signs after 30 days of treatment.

Objective:Body Mass Index

时间窗: Assessment: Percentage relief in symptoms and signs after 30 days of treatment.

次要结局

  • 1.Change in Quality-of-Life Indicators(2.Improvement in Functional Capacity)

研究者

发起方
Jammu Institute Of Ayurveda And Research
申办方类型
Research institution and hospital
责任方
Principal Investigator
主要研究者

Dr Apurva Gupta

Jammu Institute Of Ayurveda And Research

研究点 (1)

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