AN EFFECT OF JATAMANSYADI VATI IN ESSENTIAL HYPERTENSION

Phase 1/2

Recruiting

• Conditions: Vyanabala Vriddhi

• Registration Number: CTRI/2014/10/005085
• Lead Sponsor: Institute for Post Graduate Teaching And Research in Ayurveda

Brief Summary

This is a randomized control clinical trial at I P G T and R A, Gujarat Ayurved University, Jamnagar in Department of Kayachikitsa OPD. Dealing with treatment of Vyanabala Vriddhi (essential hypertension). In present study Jatamansyadi Vati which contain Jatamansi, Ashwagandha, Arjuna, Gokshura and Brahmi in equal parts will be given 1 gm BD for 28 days as interventional group. In control group Metoprolol will be given 25 mg or 50 mg OD for 28 days.

Detailed Description

Not available

Study Timeline

• Last Update Posted: 2014-02-10
• Study Start: 2014-07-04

Recruitment & Eligibility

• Status: Open to Recruitment
• Sex: All
• Target Recruitment: 40

Inclusion Criteria

Patients above 25 years and below 65 years of age will be selected for the study Patients with systolic blood pressure above 140 mm of Hg and below 180 mm of Hg will be taken for the study Patients with diastolic blood pressure above 90 mm of Hg and below 110 mm of Hg will be taken for the study Patients presenting with the classical symptoms of Hypertension will be taken for the study.

Exclusion Criteria

Patients below 25 years and above 65 years of age will be excluded from the study Patients with systolic blood pressure below 140 mm of Hg and above 180 mm of Hg will be excluded from the study Patients with diastolic blood pressure below 90 mm of Hg and above 110 mm of Hg will be excluded from the study Patients having major illness like severe D.M., tuberculosis, major endocrine disorders, malignancies, HIV, renal failure will be excluded from the study Patients having accelerated and malignant hypertension and history of cardiac compromise like angina, MI, CCF will also be excluded.

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
control of hypertension	28 days

Secondary Outcome Measures

Name	Time	Method
improve quality of life	after 28 days

Trial Locations

Locations (1)

OPD Department of Kayachikitsa; 🇮🇳 Jamnagar, GUJARAT, India

OPD Department of Kayachikitsa

🇮🇳Jamnagar, GUJARAT, India

Shreyas Rajeshkumar Adhvaryu

Principal investigator

9913063278

shreyasadhvaryu@yahoo.co.in