A Randomized Controlled Trial to evaluate the efficacy of Hapushadi Yapana Basti with Tila Taila Matra Basti in the management of Sandhigata Vata with special reference to Katishoola.

Sane Guruji arogya Kendra1 个研究点分布在 1 个国家目标入组 60 人开始时间: 2026年2月16日最近更新: 2026年1月27日

试验速览

阶段: 不适用
状态: 尚未招募
发起方: Sane Guruji arogya Kendra
入组人数: 60
试验地点: 1

研究概览研究设计入排标准研究者研究点记录与标识符相似试验

研究概览

简要总结

This is randomized controlled trial to evaluate the efficacy of Hapushadi Yapana Basti by comparing with the control drug Tila taila matra basti. Trial group will be given Hapushadi yapana basti from 2nd to 6th day and tila taila matra basti will be given on 1st and 7th day. Control group will be given Tila taila matra basti for continuous 7 days. Observations will be drawn from outcome of patient.

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: 20.00 Year(s) 至 60.00 Year(s)（—）
性别: All

入选标准

•Basti arha Patients diagnosed with Katishoola.
•Patients with non-specific, mechanical, or degenerative low back pain (e.g., k/c/o lumbar spondylosis, myofascial pain, postural LBP).

排除标准

•Patients having congenital structural deformities.
•Patients having other joint deformities or diseases which are not related to Katishoola.
•K/C/O Sciatica will be excluded.
•Neurological signs of radiculopathy, spinal trauma, infection, malignancy, severe stenosis.
•Patients with systemic disease which may cause interference in the treatment of study will be excluded.
•o Pregnant women.

研究者

发起方

Sane Guruji arogya Kendra

申办方类型

Research institution and hospital

责任方

Principal Investigator

主要研究者

Nikita Narendra Lunkad

Sumatibhai Shah Ayurved Mahavidyalaya

研究点 (1)

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