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临床试验/CTRI/2026/02/103084
CTRI/2026/02/103084尚未招募4 期

EFFECT OF SIDDHA VASTI IN THE MANAGEMENT OF GRADE 1 AND 2 NON - ALCOHOLIC FATTY LIVER DISEASE (NAFLD)

Government Ayurveda College Tripunithura1 个研究点 分布在 1 个国家目标入组 25 人开始时间: 2026年2月18日最近更新:

试验速览

阶段
4 期
状态
尚未招募
发起方
入组人数
25
试验地点
1

研究概览

简要总结

Non-Alcoholic Fatty Liver Disease (NAFLD) is a prevalent lifestyle related hepatic disorder marked by abnormal accumulation of fat in the liver. If not addressed at an early stage, it may progress to advanced conditions such as fibrosis, cirrhosis, and hepatocellular carcinoma. At present, there is no established definitive pharmacological therapy for early stage NAFLD, Emphasizing the need to explore alternative treatment modalities. From an Ayurvedic perspective, NAFLD can be understood in relation to Santarpanajanya Vyadhi and Medoroga, Wherein deranged Agni along with vitiation of Kapha and Meda plays a central role in the disease pathogenesis. Siddha Vasti, as described in classical Ayurvedic literature, is known to possess Kapha Medohara, Lekhana, and Srotoshodhana properties, which may be beneficial in the management of NAFLD. This study is designed as a single arm, interventional pre and post test clinical trial involving 25 participants aged between 25 and 55 years, diagnosed with Grade 1 and Grade 2 NAFLD. Siddha Vasti will be administered for 7 consecutive days. Clinical and biochemical assessments will be carried out at baseline, on the 8th day, and on the 22nd day using the NAFLD fibrosis score, liver function tests, and lipid profile. While ultrasonography of abdomen will be carried out at baseline and on 22 nd day . Samyak Lakshanas of niruha vasti will be assessed daily. The primary objective of the study is to evaluate the effectiveness of Siddha Vasti in improving fibrosis scores and reducing the severity of NAFLD. The outcomes of this study may contribute to scientific evidence, supporting the role of Panchakarma therapy, particularly Siddha Vasti, in the management of early stage NAFLD.

研究设计

研究类型
Interventional
分配方式
Na
盲法
None

入排标准

年龄范围
25.00 Year(s) 至 55.00 Year(s)(—)
性别
All

入选标准

  • Subject with NAFLD Grade 1 And 2 Subjects within the age group of 25 To 55 years Subjects fit for Niruha Vasti Subjects who will give written consent.

排除标准

  • Participants with Major Systemic illness Participants with Malignancy Participants with Portal Hypertension Participants with Splenomegaly Pregnant and lactating women.

研究者

发起方
Government Ayurveda College Tripunithura
申办方类型
Government medical college
责任方
Principal Investigator
主要研究者

Muley Pratik Pradeep

Government Ayurveda College And Hospital Tripunithura

研究点 (1)

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