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A Comparative Clinical Evaluation of Savitri Pranayama and Om Chanting on different health variable in the cases of Stage 1st Hypertension

A Comparative Clinical Evaluation of Savitri Pranayama and Om chanting on different health variable in the cases of Stage 1st Hypertension

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/05/052363
Enrollment
120
Registered
2023-05-08
Start date
Unknown
Completion date
Unknown
Last updated
2023-05-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: I10- Essential (primary) hypertension

Interventions

Intervention1: Group 1 - Savitri Pranayama Group 2 - Om chanting Group 3 - Savitri Pranayama along with hypertension: 1. Savitri Pranayama - 30 min 2. om chanting - 30 min 3. Savitri pranayama along

Sponsors

Department of Kayachikitsa Faculty of Ayurveda Institute of Medical Science
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: People with 1 who are willing to give consent to participate in the study 2 stage 1st Hypertension 3 Age group between 30-50 years irrespective of sex religion occupation and socioeconomic status

Exclusion criteria

Exclusion criteria: Patients with 1 140/90 mmHg 2 age limits >50 and 3 diabetic mellitus and thyroid disorder 4 significant cardiovascular and respiratory system complications 5 No major illness affects the autonomic nervous system 6 Habits of chewing tobacco smoking and alcoholism 7 chronic disease 8 steroid medicine 9 lactation females are excluded 10 psychological error 11 people not willing to participate in the study or not in a position to give consent

Design outcomes

Primary

MeasureTime frame
1 Blood pressure 2 Stress 3 Sleep 4 BMI 5 Heart rate 6 Respiratory rate 7 vital capacity 8 subjective parameter such as headache, chest pain, dizziness, sleep, polyuria, blur vision, nausea, palpation 4 changes in subjective and objective parametersTimepoint: 63 days with three follow up on 21 days

Secondary

MeasureTime frame
Complete Blood Count (CBC) Lipid profile Renal Function Test Liver Function Test Timepoint: 63 days before and after trial

Countries

India

Contacts

Public ContactDr Ajai Kumar Pandey

Banaras Hindu University Varanasi

drajaipandey@gmail.com9452827885

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026