跳至主要内容
临床试验/CTRI/2025/10/096474
CTRI/2025/10/096474尚未招募2/3 期

A comparative study to evaluate the efficacy of Gandh tail with Dashmool majja basti in the management of Asthimajjagata vat w.s.r. to Avascular Necrosis of femoral head .

Dr Shwetal Shivhare1 个研究点 分布在 1 个国家目标入组 46 人开始时间: 2025年11月10日最近更新:

试验速览

阶段
2/3 期
状态
尚未招募
发起方
入组人数
46
试验地点
1
主要终点
After the completion of therapy we will able to conclude the role of Gandh tail and majja basti describe in our classic on bone and joint disorder like AVN

研究概览

简要总结

The present clinical study aims to evaluate the efficacy of Gandha Taila in combination with Dashmooladi Majja Basti in the management of Asthimajjagata Vata with special reference to Avascular Necrosis (AVN) of the Femoral Head. The trial seeks to assess improvements in pain, joint mobility, and functional outcomes, and to explore the potential of this Ayurvedic management protocol as a safe and effective alternative or adjunct therapy for AVN patients.

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
20.00 Year(s) 至 50.00 Year(s)(—)
性别
All

入选标准

  • Patients willing to participate in the trial Patients between the age group of 20-50 year of either sex or religion Diagnosed case of Avascular necrosis with grade I to grade III Diagnosed case of Avascular necrosis of femoral head with X-ray hip joint or CT scan or MRI of hip joint will be included in this study.

排除标准

  • Patients unwilling to participate in the trial Patients age are not less than 20 years or above 50 years Diagnosed case of Avascular necrosis with grade IV Patients suffering from cardiac disease and Severe lung disease Endocrine disease like Cushing syndrome and sle sickle cell anemia Patients with HIV Positive and having tuberculosis Pregnant and lactating mothers should be excluded Patients without written consent form.

结局指标

主要结局

After the completion of therapy we will able to conclude the role of Gandh tail and majja basti describe in our classic on bone and joint disorder like AVN

时间窗: Total duration 18 months and 3 month for control group

次要结局

未报告次要终点

研究者

发起方
Dr Shwetal Shivhare
申办方类型
Other [self]
责任方
Principal Investigator
主要研究者

Dr Shwetal Shivhare

Parol Institute of Ayurveda Parol Univercity Vadodara Gujarat

研究点 (1)

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