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临床试验/CTRI/2025/06/089716
CTRI/2025/06/089716尚未招募2 期

Efficacy and Safety of Habbe Gule Aak versus Habbe Suranjan in Primary Gout A Comparative Clinical Study

Govt Tibbi College And Hospital1 个研究点 分布在 1 个国家目标入组 30 人开始时间: 2025年7月15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
30
试验地点
1
主要终点
Reduction of serum uric acid

研究概览

简要总结

After thorough screening, diagnosed patients of primary gout who fulfil inclusion criteria will be included in study. Patients will be included for the study. The patients will be randomly allocated in two groups 30 in test group (Habbe Gule Aak) and 30 in control group (Habbe Suranjan). Treatment will be given for 30 days in both groups. Objective Parameters will be assessed before and after treatment.

研究设计

研究类型
Interventional
分配方式
Coin toss, Lottery, toss of dice, shuffling cards etc
盲法
None

入排标准

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

入选标准

  • 1.Diagnosed cases of primary gout 2.serum uric acid more than 7.2% 3.Patients of either gender 4.Patients between 30 to 65 years of age Patients who have agreed to participate and sign the consent form.

排除标准

  • 1.Pregnancy and lactation 2.Complicated cases of Gout 3.Co-morbid conditions of participants like Diabetic Ketoacidosis, Nephropathy, Coronary artery disease, Peripheral vascular disease, cerebrovascular disease and liver disease.
  • 4.Immuno-compromised states like Malignancies, AIDS and on Immuno-suppressive agents.
  • 5.Participants fail to attend treatment schedule regularly.

结局指标

主要结局

Reduction of serum uric acid

时间窗: at baseline i.e. 00th day(visit 1 ,7th day(visit 2), 14th day ( visit 3) and 30th day ( visit 4)

次要结局

  • Change in different clinical symptoms of primary gout(7th, 14th, 21st, and 30th days)

研究者

发起方
Govt Tibbi College And Hospital
申办方类型
Government medical college
责任方
Principal Investigator
主要研究者

DR HELAL ANWER

GOVERNMENT TIBBI COLLEGE AND HOSPITAL

研究点 (1)

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