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临床试验/CTRI/2016/04/006848
CTRI/2016/04/006848进行中(未招募)2 期

External application of Siddha medicine- Moosambara patru on Mootu veekam (Swollen Knee joint) – Short term Clinical Trial

Central Council for Research in Siddha1 个研究点 分布在 1 个国家目标入组 30 人开始时间: 2015年2月28日最近更新:
适应症

试验速览

阶段
2 期
状态
进行中(未招募)
发起方
入组人数
30
试验地点
1
主要终点
To assess the changes in the swelling of the subjects by measuring the circumference of the affected joint before and after treatment

研究概览

简要总结

Based on the Case sheet proforma the trial subjects wererecruited for the trial. At first they were sent for screening whether to confirmthe diagnosis. The consent forms signed by the patients were collected and thePatient information sheet was given as per the ethical guidelines. They wereasked to report to the Investigators every 5days once for a consecutive periodof 15days. The recruited patients were enrolled in the register. Theinvestigations were advised as per the protocol. The Moosambara patru25 g ofmedicine was given to the patients with subject I.Dnos. They were asked to Applied the medicine in swollen joint for 5 days mixedwith White Egg yolk as a External therapy .And every visit measuring the swollen knee joints with helpof non elastic inch tap, before and after treatments. Every five days onceMeasurements were done consecutively for a period of 15days treatment.The data generated maintained in the excel sheet.

研究设计

研究类型
Interventional
分配方式
Not Applicable
盲法
Open Label

入排标准

年龄范围
40.00 Year(s) 至 65.00 Year(s)(—)
性别
All

入选标准

  • •1.Age between 40 years to 65 years 2.Patients with knee joint swelling (Single or Both knees) 3.Pain 4.Joint tenderness 5.Patients willing to give consent to participate in the trial.

排除标准

  • •1.Age less than 40 years or more than 65 years 2.Patients with Diabetes mellitus/ Hepatic failure/ Renal failure, 3.Any serious underlying infectious conditions and Hematoma 4.History of surgical interventions 5.Patients not willing to give consent to participate in the trial.

结局指标

主要结局

To assess the changes in the swelling of the subjects by measuring the circumference of the affected joint before and after treatment

时间窗: To assess the changes in the swelling of the subjects by measuring the circumference of the affected joint before and after treatment

次要结局

  • To assess the safety of the trial drug while applying externally

研究者

发起方
Central Council for Research in Siddha
申办方类型
Research institution

研究点 (1)

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