Evaluation of the effects of a Polyherbal compound in the treatment of hypertensio

Phase 2

Recruiting

• Conditions: Hypertensive.; Hypertensive diseases; I10-I15

• Registration Number: IRCT2016110225772N4
• Lead Sponsor: Esfarayen University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 17 August 2020

Recruitment & Eligibility

• Status: Recruiting
• Sex: All
• Target Recruitment: 550

Inclusion Criteria

1. The desire to participate in the study, 2. Men and Women between 25-65 years, 3 patients with mild hypertension, 4-lack of heart disease, 5-lack of kidney disease

Exclusion Criteria

Not provided

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Diastolic blood pressure. Timepoint: Before intervention,one month after intervention. Method of measurement: questionnaire.;Diastolic blood pressure. Timepoint: Before intervention,one month after intervention. Method of measurement: questionnaire.;LDL. Timepoint: Before intervention,one month after intervention. Method of measurement: Blood examination.;HDL. Timepoint: Before intervention,one month after intervention. Method of measurement: Blood examination.;Total cholestrol. Timepoint: Before intervention,one month after intervention. Method of measurement: Blood examination.;Triglyceride. Timepoint: Before intervention,one month after intervention. Method of measurement: Blood examination.