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临床试验/CTRI/2025/08/092323
CTRI/2025/08/092323尚未招募2 期

A Pharmaco clinical Study To Evaluate The Efficacy Of Ashwagandha Ghrita (Withania somnifera Linn) and Bala Tail(Sida cordifolia Linn) in Janu Sandhivata wsr to Knee Osteoarthritis

State Ayurvedic College and Hospital, Lucknow1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2025年8月22日最近更新:

试验速览

阶段
2 期
状态
尚未招募
发起方
入组人数
60
试验地点
1
主要终点
1. pain in joints

研究概览

简要总结

A OA patient experiences difficulty in persuing in day to day activity. therefore , i select this trial . this research evaluate the efficacy of ashwagandha ghrita & bala tail. this research  is parallel group randomised clinical study of 60 patients.

group A (n=30)- the patients will be given ashwagandha ghria (6gm) twice a day with lukewarm water after meal.

group B(n=30)- the patients will be given bala tail for abhyang as local application(min 5 min) twice a day & ashwagandha ghrita(6gm) with lukewarm water twice a day after meal

duration of trail - 2 months

follow up - the follow up conducted during study period for once in 15 days. after completion of trial of 2 months , the follow up without drug after 15 days for one month.

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
40.00 Year(s) 至 70.00 Year(s)(—)
性别
All

入选标准

  • 1 Age group between 40 to 70 years 2 The patients with classical signs and symptoms of sandhivata given in various texts as well as the clinical features of disease of OA given in Modern medicine 3 Patient who gave the consent to participate in study.

排除标准

  • 1 Age group less than 30 years and more than 70 years 2 Patients having past history or actively suffering from other inflammatory disease like RA Gout Septic Arthritis etc 3 Cases with severe deformities of joint and having major complications are excluded 4 Pregnant and lactating women 5 Patients having substantial abnormalities in Hematological Hepatic Metabolic function and systemic disorders like Diabetes and Hypertension 6 Avaranjanya Sandhivata.

结局指标

主要结局

1. pain in joints

时间窗: - the follow up conducted during study period for once in 15 days. | After completion of trial of two month, the follow up without drug after 15th day

2. crepitus

时间窗: - the follow up conducted during study period for once in 15 days. | After completion of trial of two month, the follow up without drug after 15th day

3. pain during extension and flexion

时间窗: - the follow up conducted during study period for once in 15 days. | After completion of trial of two month, the follow up without drug after 15th day

4. loss of motion and range

时间窗: - the follow up conducted during study period for once in 15 days. | After completion of trial of two month, the follow up without drug after 15th day

5. swelling in affected joint

时间窗: - the follow up conducted during study period for once in 15 days. | After completion of trial of two month, the follow up without drug after 15th day

6. morning stiffness(less than half an hour)

时间窗: - the follow up conducted during study period for once in 15 days. | After completion of trial of two month, the follow up without drug after 15th day

7. tenderness of joint

时间窗: - the follow up conducted during study period for once in 15 days. | After completion of trial of two month, the follow up without drug after 15th day

次要结局

  • 1. CBC, ESR(2. Blood sugar (HbA1c/random/fasting/pp))

研究者

发起方
State Ayurvedic College and Hospital, Lucknow
申办方类型
Government medical college
责任方
Principal Investigator
主要研究者

Rahul Kumar

State Ayurvedic College and Hospital, Lucknow

研究点 (1)

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