A Randomised controlled clinical study to evaluate the efficacy of Ayurvedic formulation in the management of primary hypertension

A Randomized controlled clinical study to evaluate the efficacy of Ayurvedic formulation formulation in the management of primary hypertension

Status

Active, not recruiting

Phases

Phase 2

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2025/01/078845

Enrollment

Registered

2025-01-16

Start date

Unknown

Completion date

Unknown

Last updated

2026-09-14

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

Conditions

None listed

Interventions

Intervention1: kwath (Decoction): Guduchi + Duralabha + Rakta chandan + Patol + Aragvadha + Shunthi + dhanyak Dose : 50ml BD Route of administration: Oral Duration: 14days Control Intervention1: Tabl

Eligibility

Inclusion criteria

Inclusion criteria: Systolic Blood pressure - less than 180 mm of Hg more than and equal to 140 mm of Hg Diastolic Blood pressure - less than 110 mm of Hg more than and equal to 90 mm of Hg newly diagnosed patients

Exclusion criteria

Exclusion criteria: Secondary hypertension Alcoholic and Drug abusers pregnant and lactating women

Design outcomes

Primary

Measure	Time frame
Reduction in Blood pressureTimepoint: 14 days with follow ups of 7th and 14th day	—

Secondary

Measure	Time frame
Reduction in symptoms of primary hypertension like headache, giddiness, fatigue, insomnia, perspiration, palpitationTimepoint: 14 days with follow ups of 7th and 14th day	—

Countries

India

Contacts

Public ContactDr Archi Saraf

Dr. D. Y. Patil College of Ayurveda and Research centre, Pimpri, PUNE

gunvantayurved@gmail.com9028321955

Outcome results