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Study of Herbal medicine in lowering blood pressure in comparison with standard medicine

Phase 2
Conditions
Health Condition 1: I10- Essential (primary) hypertensionHealth Condition 2: I10- Essential (primary) hypertension
Registration Number
CTRI/2023/03/050643
Lead Sponsor
ational Innovation Foundation India
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Yet Recruiting
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

•Age group 18-70 years , Either Sex

•Essential hypertension : Mild (Systolic BP- 140 to 159mm Hg and /or Diastolic BP- 90 to 99 mmHg) and Moderate (Systolic 160- 179mm of Hg / or Diastolic BP- 100-109)

Exclusion Criteria

1.History of coronary artery disease, myocardial infarction, stroke, transient ischemic attack, any revascularization procedure, congestive heart failure, or hemodynamically significant carotid or peripheral arterial disease

2.Pregnant / Breast feeding women.

3.Women having hormonal contraception or having no effective birth control measure.

4.Diabetes mellitus type I and II

5.As per the opinion of investigator ,any other Surgical /medical illness not mentioned in the protocol - which may place patients at high risk due to their participation in the study OR may lead to their noncompliance to the protocol.

6.Use of other concomitant medications â?? adrenergic drugs or steroids that may affect blood pressure.

7.Hypersensitivity to any of the test drug

8. Patients with kidney or liver disease

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
OWERING OF BLOOD PRESSURETimepoint: â?¢ Follow up: Every 7th day for upto 1 month and <br/ ><br>every 15th day after one month the patients will <br/ ><br>be observed for subjective and objective <br/ ><br>parameters will be recorded.
Secondary Outcome Measures
NameTimeMethod
Blood pressure in normal limits is sustainedTimepoint: â?¢ Follow up: Every 7th day for upto 1 month and <br/ ><br>every 15th day after one month the patients will <br/ ><br>be observed for subjective and objective <br/ ><br>parameters will be recorded. <br/ ><br>
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