跳至主要内容
临床试验/CTRI/2025/10/096000
CTRI/2025/10/096000尚未招募不适用

A Comparative Clinical Study to Evaluate the Efficacy of Kokilaksha Paneeya Kshara and Yava Paneeya Kshara in the Management of Pittashmari Cholelithiasis

Dr Patil Spoorti Gurubasav1 个研究点 分布在 1 个国家目标入组 40 人开始时间: 2025年10月20日最近更新:

试验速览

阶段
不适用
状态
尚未招募
发起方
入组人数
40
试验地点
1
主要终点
To evaluate the efficacy of treatment in reducing the size of gallstones by ultrasonographic assessment before and after 30 days Additionally to assess symptomatic relief including right upper quadrant abdominal pain

研究概览

简要总结

The present study title, " A  comparative clinical study to evaluate the efficacy of Kokilaksha paneeya kshara and Yava paneeya kshara in the management of Pittashmari (Cholelithiasis)" will be conducted on 40 subjects, with 20 in each group, with the mentioned objective and subjective parameters.  One group will be treated with Kokilaksha paneeya kshara, and the other group with Yava paneeya kshara. Assessment of the patient will be done before and after treatment

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

入选标准

  • Patients with the clinical features of Cholelithiasis or silent gallstones And Subjects of either sex and age group between 17-65 years.

排除标准

  • Patients unfit for Paneeya Kshara, immunocompromised (HIV, Hepatitis B,C), with uncontrolled systemic diseases (DM, HTN), gallstone complications such as cholecystitis, empyema, perforation, mucocele, choledocholithiasis, CBD obstruction, obstructive jaundice, cholangitis, carcinoma, pancreatitis, liver failure, any condition presenting sign of jaundice were excluded.Subjects with congenital hepatobiliary anomalies and hemolytic disorders like sickle cell anemia, thalassemia, malaria, cirrhosis, and hereditary spherocytosis are excluded.

结局指标

主要结局

To evaluate the efficacy of treatment in reducing the size of gallstones by ultrasonographic assessment before and after 30 days Additionally to assess symptomatic relief including right upper quadrant abdominal pain

时间窗: 1 month

次要结局

  • To assess the effect of treatment on symptomatic relief including nausea vomiting flatulence and dyspepsia Additionally to evaluate tenderness(4 months)

研究者

发起方
Dr Patil Spoorti Gurubasav
申办方类型
Other [self]
责任方
Principal Investigator
主要研究者

Dr Patil Spoorti Gurubasav

Dr N A Magadum Ayurvedic Medical College Hospital And Research Centre, Ankali

研究点 (1)

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