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â??A Clinical Study to Evaluate the Efficacy of Ayurvedic formulations NIA/DG/2015/01 and NIA/DG/2020/01 along with Walking in the Management of Newly Diagnosed Primary Hypertension.â??

Phase 3
Conditions
Health Condition 1: I10- Essential (primary) hypertension
Registration Number
CTRI/2022/11/046970
Lead Sponsor
ational Institute of Ayurveda Jaipur Rajasthan
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

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

1.Patients belonging to both sexes between the age group 18 to 60 years without major comorbidities.

2.Patients who already diagnosed as primary hypertension & not taking any antihypertensive medication will be selected.

3.Duration of disease- 1-3 month. (Patients whose primary hypertension has been diagnosed before 3 months from the date of screening for this trial will be considered as newly diagnosed cases of primary hypertension.)

4.Mild to moderate grade patients of hypertension as per 8th JNC.

5.Patients having systolic blood pressure >=140 upto 180 mm of hg and diastolic blood pressure >= 90 upto 110 mm of hg will be selected for the study.

6.Patients who are willing to fill the informed consent form.

7.Patients who are willing to download suitable mobile applications to record their walking program.

Exclusion Criteria

1.Known cases of Secondary hypertension, renal diseases, Diabetic Mellitus.

2.Known cases of Pregnancy induced hypertension.

3.Known cases of Ventricular hypertrophy, coarctation of aorta, Portal hypertension, and renal artery stenosis induced hypertension.

4.Patients using other antihypertensive medicines of conventional biomedicine / AYUSH systems / any other system.

5.Patients using drugs like Oral Contraceptive Pills, steroids.

6.Patient with no evidence of any target organ damage.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Reduction the high systolic and diastolic blood pressure to normal range.Timepoint: Blood pressure will be recorded at 15th days,30,45,60,75,90 day
Secondary Outcome Measures
NameTimeMethod
Improvement in the subjective parameters of primary hypertension.Timepoint: at 15,30,45,60,75,90 day
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