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Effect of a New Ayurvedic Formulation NIA/DG/2020/01 on High Blood Pressure

CLINICAL EVALUATION OF A NEW AYURVEDIC FORMULATION [NIA/DG/2020/01] IN STAGE -1 PRIMARY HYPERTENSION

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2021/04/033231
Enrollment
60
Registered
2021-04-29
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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: NIA/DG/2020/01 - trial drug of study : Dose- 2 capsules twice a day Anupana- Lukewarm water Route of administration- Oral Time of administration- Before meal Duration of therapy- 90 day

Sponsors

National Institute of Ayurveda
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Patients belonging to either sex between the age group 18 to 60 years. 2. Patients of Stage 1 Primary Hypertension. 3. Mild to moderate grade patients of hypertension as per 8th JNC & WHO criteria will be included. 4. Isolated grade-1 systolic or diastolic hypertension.

Exclusion criteria

Exclusion criteria: 1. Known cases of Secondary hypertension. 2. Known cases of Renal diseases, Diabetic Mellitus. 3. Known cases of Pregnancy induced hypertension. 4. Known cases of Ventricular hypertrophy, coarctation of aorta. 5. Known cases of Portal hypertension. 6. Known cases of Renal artery stenosis induced hypertension. 7. Patients using other antihypertensive medicines of conventional biomedicine / AYUSH systems / any other system. 8. Patients using drugs like Oral Contraceptive Pills, steroids. 9. Patient not taking any previous anti-hypertensive medication. 10. Patient with no evidence of any target organ damage.

Design outcomes

Primary

MeasureTime frame
Reduction in Blood PressureTimepoint: Reduction in blood pressure after 2 weeks, 4 weeks, 6 weeks, 8 weeks, 10 weeks, 12 weeks.

Secondary

MeasureTime frame
Changes in Sign and symptom (Subjective Criteria) Changes in Objective Criteria like DLC, Platelet count, SGOT, SGPT & S. Creatinine.Timepoint: 3 months follow up 1 month

Countries

India

Contacts

Public ContactDr Swati Goyal

National Institute of Ayurveda

sudipt@gmail.com9828376668

Outcome results

None listed

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