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临床试验/CTRI/2024/12/078222
CTRI/2024/12/078222尚未招募不适用

Usefulness of boger boenninghausen’s characteristics and repertory in homoeopathic management of hyperuricemia by considering rubric uric acid diathesis a prospective single arm pre post clinical study

Bakson Homoeopathic Medical College and Hospital2 个研究点 分布在 1 个国家目标入组 35 人开始时间: 2024年12月30日最近更新:

试验速览

阶段
不适用
状态
尚未招募
发起方
入组人数
35
试验地点
2
主要终点
It is expected that there will be reduction in serum uric acid level of patients.

研究概览

简要总结

This is an prospective observational study to assess the effect of boger boenninghausen’s characteristics and repertory in homoeopathic management of hyperuricemia by considering rubric uric acid diathesis

Sample size of the study is 35

It is expected that there will be reduction in serum uric acid level of patients.

There will be improvement in patient’s outcome without any substantial medical adverse effect hence a significant reduction in serum uric acid level is expected as compared to baseline and at end of 6 months.

研究设计

研究类型
Interventional
分配方式
Na
盲法
None

入排标准

年龄范围
18.00 Year(s) 至 59.00 Year(s)(—)
性别
All

入选标准

  • Participants of age group 18-59 year Male with SUA level more than 7 mg/dl and female with more than 6.0 mg/dl Participants willing to give consent will be included Uric acid diathesis as Eliminating Rubric.

排除标准

  • Participants with unstable mental or psychiatric diseases, uncontrolled or severe systemic illnesses, substance abuse, severe endocrine disorders, and already receiving homeopathic treatment for any chronic condition for past 3 months Pregnant and lactating females Recurrent case of renal stone.

结局指标

主要结局

It is expected that there will be reduction in serum uric acid level of patients.

时间窗: 15 months study | Enrollment – 6 months | follow up – 6 months | Statistical analysis – 3 months | first dose after case taking subsequent doses as per follow ups

There will be improvement in patient’s outcome without any substantial medical adverse effect hence a significant reduction in serum uric acid level is expected as compared to baseline and at 6 months.

时间窗: 15 months study | Enrollment – 6 months | follow up – 6 months | Statistical analysis – 3 months | first dose after case taking subsequent doses as per follow ups

次要结局

未报告次要终点

研究者

发起方
Bakson Homoeopathic Medical College and Hospital
申办方类型
Private medical college
责任方
Principal Investigator
主要研究者

Dr Anjali Khanai

Bakson Homoeopathic Medical College and Hospital

研究点 (2)

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