To study the effect of Vidanga capsules in high cholesterol condition

To study the efficacy of Vidanga extract capsules in dyslipidaemia w.s.r. to Shonitabhishyanda- A double blind randomized controlled clinical trial - Nil

Status

Recruiting

Phases

Phase 1Phase 2

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2025/12/099267

Enrollment

Registered

2025-12-16

Start date

Unknown

Completion date

Unknown

Last updated

2026-08-03

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

Conditions

Health Condition 1: E65-E68- Overweight, obesity and other hyperalimentation

Interventions

None listed

Eligibility

Inclusion criteria

Inclusion criteria: Individuals diagnosed with dyslipidaemia Age group 35 to 60 years of age Subjects willing to give written consent

Exclusion criteria

Exclusion criteria: Hypertension Diabetes mellitus Hypothyroidism Pregnancy and lactation Other systemic illnesses and addictions

Design outcomes

Primary

Measure	Time frame
To study the efficacy of Vidanga extract in dyslipidaemiaTimepoint: 2 months sample size 40	—

Secondary

Measure	Time frame
Secondary Objectives: a) To study the efficacy of Vidanga extract on anthropometric parameters b) To study the efficacy of Vidanga extract on quality of lifeTimepoint: Duration of study: 2 months	—

Countries

India

Contacts

Public ContactDr Sowmya Bhat

SDM College of Ayurveda Hospital and Research Centre Kuthpady Udupi

sapre.soumya@gmail.com9900846287

Outcome results