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An Observational Study to Assess Ayurvedic Pathogenesis of Hypertension

An Observational Study to Assess Ayurvedic Pathogenesis (Samprapti) of Hypertension - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2025/02/081117
Enrollment
201
Registered
2025-02-21
Start date
Unknown
Completion date
Unknown
Last updated
2025-03-03

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

None listed

Sponsors

Dr Suyog Jawake
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Pre diagnosed patient of hypertension Hypertensive patients of all three grades

Exclusion criteria

Exclusion criteria: Patient having hypertension but not willing to participate in study

Design outcomes

Primary

MeasureTime frame
The primary outcome of this study is the assessment of the Ayurvedic pathogenesis (Samprapti) of hypertension based on Ayurvedic parameters, including Dosha, Dushya and Srotas involvement in 201 individuals diagnosed with hypertension.Timepoint: As this is a cross-sectional study, the outcome will be assessed at a single time point (i.e., at the time of participant recruitment and data collection).

Secondary

MeasureTime frame
The secondary outcome of this study is to assess & analyze the potential etiological factors (Nidana) contributing to hypertension in 201 individuals, based on Ayurvedic principles.Timepoint: As this is a cross-sectional study, the secondary outcome will be assessed at a single time point (i.e., at the time of participant recruitment & data collection).

Countries

India

Contacts

Public ContactDr Suyog Jawake

Dr.D.Y.Patil College of Ayurveda & Research Centre Pimpri Pune

mrudula.joshi@dpu.edu.in9226279270

Outcome results

None listed

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