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临床试验/CTRI/2026/01/101462
CTRI/2026/01/101462尚未招募3 期

A Randomized Clinical Study Comparing The Efficacy Of Shashtika Shali Pinda Swedana With Panchatikta Panchaprasritik Basti Vs Sarvanga Abhyanga In Diabetic Peripheral Neuropathy

National Institute Of ayurveda1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2026年7月1日最近更新:

试验速览

阶段
3 期
状态
尚未招募
入组人数
60
试验地点
1

研究概览

简要总结

This randomized, active-controlled clinical study is designed to compare the efficacy of Shashtika Shali Pinda Swedana with Panchatikta Panchaprasritika Basti versus Sarvanga Abhyanga in patients suffering from Diabetic Peripheral Neuropathy. Eligible participants will be randomly allocated into two groups. Group A will receive Basti Karma using Panchatikta Panchaprasritika Basti (500 ml, rectal route, administered in the morning on an empty stomach) along with Shashtika Shali Pinda Swedana preceded by Guduchyadi Taila Abhyanga, administered daily for 15 days. Group B will receive Sarvanga Abhyanga with Guduchyadi Taila for 30 minutes daily for 15 days. The total duration of the clinical trial is 15 days, with a follow-up assessment conducted after 30 days post-treatment to evaluate the sustainability of therapeutic effects. The study aims to assess and compare the clinical efficacy of these Ayurvedic interventions in the management of diabetic peripheral neuropathy.

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 70.00 Year(s)(—)
性别
All

入选标准

  • Patients diagnosed with diabetic peripheral neuropathy
  • Participants willing and able to participate in this study for entire trial period with informed consent.
  • Participants fit for basti, shalishastikapindaswedana and sarvangaswedana.

排除标准

  • Patient, suffering from any acute or chronic debilitating disease (conditions involving cardiac, vascular, hematological, respiratory, hepatic, gastrointestinal, renal functions,central nervous system.
  • or psychiatric disorder or active cancer).
  • Type 1 Diabetes Mellitus or Uncontrolled diabetes mellitus
  • Patients with long term steroid treatment.
  • Participants Not fit for Basti, ShaliShastikaPindaswedana and SarvangaSwedana.

研究者

申办方类型
Other [National Institute of Ayurveda (De Novo), Ministry of Ayush, Govt of India]
责任方
Principal Investigator
主要研究者

Dr Jitendra Shakya

National Institute Of ayurveda

研究点 (1)

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