Effectiveness of Viscum Album Mother Tincture as an Anti-hypertensive in Essential Hypertension

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

37 participants

Study Classification

INTERVENTIONAL

Study Start Date

2011-02-28

Study Completion Date

2011-09-30

Brief Summary

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To estimate the effectiveness of Viscum album Homoeopathic mother tincture in Essential Hypertension by conducting clinical trial in moderate hypertensive patients for a period of six weeks.

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Detailed Description

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Conditions

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Hypertension

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Interventions

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Viscum album ethanolic extract manufactured according to Homoeopathic pharmacopoeia of India (H.P.I.)

Ten drops of Drug in 30 ml of distilled water with a frequency of three times a day for a duration of 12 weeks

Intervention Type DRUG

Eligibility Criteria

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Inclusion Criteria

* Hypertension at the range 180-120 mm of Hg for Systole \&
* 110-80 mm of Hg for Diastole

Exclusion Criteria

* Patients who are on ACEI / ARB for Hypertension
* Diseases in which life expectancy is less than six months
* Secondary hypertension
* CHD
* Family History of Mental Illness like Anxiety or depression.
* Nasal Congestion

Minimum Eligible Age

40 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No