Efficacy Of Homoeopathic Medicines Using LM Potency in Management Of Essential Hypertension(Grade 1) in Patients having Body Mass Index 25-35
试验速览
- 阶段
- 2 期
- 状态
- 已完成
- 发起方
- 入组人数
- 40
- 试验地点
- 1
- 主要终点
- changes in the blood pressure both systolic and diastolic
研究概览
简要总结
This study is a prospective pre test post test interventional trial to assess the efficacy of Homoeopathic medicines in LM potency in 40 participants of grade 1 hypertension BMI 25-35 as per the inclusion criteria and exclusion criteria from OPD The Primary outcome will assess the changes in Blood pressure after giving Individual Homoeopathic medicines in LM potency at 2 4 6 8 months.
Secondary outcome will assess changes in MINICHAL Questionnarie after giving Individual Homoeopathic medicines in LM potency from baseline and at the end of treatment .
研究设计
- 研究类型
- Interventional
- 分配方式
- Na
- 盲法
- Participant Blinded
入排标准
- 年龄范围
- 30.00 Year(s) 至 79.00 Year(s)（—）
- 性别
- All
入选标准
- •Participants must have a confirmed diagnosis of essential hypertension as per established medical criteria Participants with baseline Systolic Blood Pressure more than 120 to 159 and Diastolic Blood Pressure more than 80 to 99 who are not on any anti hypertensive medicines Participants with a body mass index of 25 to 35 Participants willing to provide informed consent to participate in the study and also who can fill up the Questionnaire.
排除标准
- •Patients who are suffering from secondary Hypertension of known aetiology such as renal disease pheochromocytoma or Cushing’s syndrome known diabetics, history of myocardial infarction severe coronary artery disease or clinically significant heart failure or valvular defect or known cases of cardiac diseases any systemic illness consumptive disease autoimmune disease cancer hepatic disease renal disease Patients receiving any drugs known to affect Blood Pressure or medical treatments that can influence the Blood Pressure having a history of alcohol or drug abuse Women who are taking contraceptive pills pregnancy and lactating mother Patients having class 2 and class 3 obesity.
结局指标
主要结局
changes in the blood pressure both systolic and diastolic
时间窗: data will be assessed from baseline 2 4 6 8 months and changes in the blood pressure will be assessed
次要结局
- changes in the Minichal Questinnorie score(from baseline to at the end of treatment)
研究者
DrArfana Chauhan
Smt A J Savla Homoepathic Medical college and Research Institute