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Clinical Trials/CTRI/2022/12/047939
CTRI/2022/12/047939Not yet recruitingPhase 3 4

“A clinical study to evaluate the efficacy of Takra Shirodhara along with Ksheer Bala Tail Shiro Abhyanga in the management of Raktagata Vata (Essential Hypertention)â€

Dr Sarvepalli Radhakrishnan Rajasthan Ayurved University Jodhpur1 site in 1 country30 target enrollmentStarted: October 12, 2022Last updated:
Conditions

Trial Snapshot

Phase
Phase 3 4
Status
Not yet recruiting
Sponsor
Enrollment
30
Locations
1
Primary Endpoint
Subjective Criteria

Study Overview

Brief Summary

Raktagata vata (Hypertension) is a type of Vata vyadhai, in which vitiation of Vata dosha in Rakta causes pain in whole body, increased Temprature, Vivarnta (discoloration), Krishta(emaciation), Aruchi (anorexia), Arunshika(boil) in whole body and Anna Stambha etc. symptoms appears. Most of efforts shows a prime role of Vata in association of remaining dosha pitta and kapha. Rraktagata vata somewhat resembles Hypertension. It is a disease of circulatory system, in which systemic arterial blood pressure elevate beyond the normal value (more then 130 /85mm of hg). In allopathy various Antihypertensive drugs like Beta blockers, Calcium channel blockers, Diuretics thiazide, ACE inhibitors are being used to decrease blood pressure, However these drugs are producing several Adverse Effects like feeling nervous erection problem. dizziness, feeling tired, headache, nausea or vomiting, so we looking to alternative system especially Ayurveda and find out solution to increase Blood Pressure. The study is open labelled Randomised to prove the efficacy of Takra Shirodhra along with Ksheer Bala tail Shiro abhyanga in the management of Raktagata vata (Essential Hypertension). In this Study 30 patients will be registered for Shiroabhyanga And Shirodhara.

Study Design

Study Type
Interventional
Allocation
Not Applicable
Masking
Open Label

Eligibility Criteria

Ages
35.00 Year(s) to 70.00 Year(s) (—)
Sex
All

Inclusion Criteria

  • •1.Patient With Cardinal Symptoms Of Hypertension.
  • •Patient Previously Diagnosed With Hypertension, Systolic Blood Pressure Between 140-160 Mm Of Hg (Grade 1) Within 5year Prior To Start The Trial.
  • •Patient Willing To Sign The Consent Form.

Exclusion Criteria

  • •Patients With Age Below 35 Years And Above 70year.
  • •Patient Having Secondary Hypertension.
  • •Patient With Malignant Hypertension I.E. Blood Pressure Above 200/140mm Of Hg.
  • •Having Any Other Serious Illness Like Coronary Artery Disease, Cerebrovascular Disease, Renal Function Impairment.

Outcomes

Primary Outcomes

Subjective Criteria

Time Frame: 45 days

Klama(Fatigue)

Time Frame: 45 days

Hritspandan(Palpitation)

Time Frame: 45 days

Objective Criteria

Time Frame: 45 days

Severity Scoring Of Shiroshool (Headache)

Time Frame: 45 days

Swedadhikyata(Excessive Sweating)

Time Frame: 45 days

Sphygmomanometer

Time Frame: 45 days

Bhrama (Giddiness)

Time Frame: 45 days

Anidra(Insomnia)

Time Frame: 45 days

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor
Dr Sarvepalli Radhakrishnan Rajasthan Ayurved University Jodhpur
Sponsor Class
Government medical college

Study Sites (1)

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