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临床试验/CTRI/2025/12/099211
CTRI/2025/12/099211尚未招募3 期

A Pragmatic Clinical Trial to evaluate the effectiveness of Agnikarma with Ksaudra against Agnikarma with Pancaloha salaka in De-Quervains tenosynovitis

VPSV Ayurveda College Kottakkal1 个研究点 分布在 1 个国家目标入组 34 人开始时间: 2026年1月1日最近更新:

试验速览

阶段
3 期
状态
尚未招募
发起方
入组人数
34
试验地点
1

研究概览

简要总结

De-Quervains tenosynovitis is a painful condition affecting the tendons on the radial side of

the wrist, impairing thumb movement and daily activities. In Ayurveda, this condition can be

correlated with Snayugata Vata, where Agnikarma is indicated as a primary line of treatment.

This Pragmatic Clinical Trial aims to evaluate the relative effectiveness of Agnikarma with

Ksaudra and Agnikarma with Pancaloha Salaka in managing De-Quervains tenosynovitis. A

total of 34 participants satisfying the inclusion criteria will be randomly assigned into two

groups at the Shalyatantra OPD of VPSV Ayurveda College Hospital, Kottakkal.

Group I will undergo Agnikarma with Ksaudra and Group II will undergo Agnikarma with

Pancaloha Salaka as a one-time intervention, with assessments on day 1 (before and after the

intervention), day 8, day 15, and follow-up on day 45. Outcomes will be evaluated using

clinical parameters including Visual Analogue Scale for pain, Tenderness-for primary

objective and Swelling grading, Finkelstein’s Eichhoff’s test, WHAT test, and goniometric

assessment for thumb abduction and wrist ulnar deviation for secondary objective. Data will

be analyzed using appropriate statistical tools and outcome will be presented in the form of

dissertation. The objective of this study is to determine the most appropriate Agnikarma

approach for effective clinical management of De-Quervains tenosynovitis.

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 60.00 Year(s)(—)
性别
All

入选标准

  • 1.Participants satisfying diagnostic criteria of De-Quervains tenosynovitis 2.Participants having a VAS score of atleast 4 for pain 3.participants giving written informed consent.

排除标准

  • 1.Participants who are contraindicated for Agnikarma 2.Participants with history of surgery,fractures of wrist joint and hand in the last 1 year 3.Participants with diagnosed cases of Rheumatoid arthritis and Gout 4.Pregnant women and lactating mother 5.Participants with diagnosed cases of uncontrolled Diabetes mellitus (HbA1C-greater than 7.5 percent) and uncontrolled hypertension(160/100 mmHg).

研究者

发起方
VPSV Ayurveda College Kottakkal
申办方类型
Other [Aided college]
责任方
Principal Investigator
主要研究者

Dr FAHMA JEBIN K V M

VPSV Ayurveda College,Kottakkal

研究点 (1)

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