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To evaluate effects of an ayurvedic formulation in management of increased lipid and cholesterol levels

To Evaluate Innovative Natural Formulation in Addressing Dyslipidemia (Elevated Lipids and Cholesterol) In Atherosclerotic Cardiovascular Disease (ASCVD) - NIL

Status
Active, not recruiting
Phases
Phase 2Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/05/110304
Enrollment
44
Registered
2026-05-10
Start date
Unknown
Completion date
Unknown
Last updated
2026-06-01

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

Conditions

Health Condition 1: E785- Hyperlipidemia, unspecified

Interventions

None listed

Sponsors

Dabur Research and Development Centre
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1) Male or female aged more than and equal to 30 years and less than and equal to 70 years 2) Body mass index between 18 Kgperm2 and 35 Kgperm2 3)Total cholesterol level between 200 and 280 mgperdL andor LDL-C between 130 mgperdL and 190 mgperdL TGless5percentage) 3)The intervention strategy does not require a pharmacological lipid-lowering intervention, according to any ICMR guidelines 4)Subjects who can communicate, make themselves understood and comply with the requirements of the study 5)Subjects who agree to participate in the study and have dated and signed the informed consent form

Exclusion criteria

Exclusion criteria: 1) Ongoing lipid lowering therapy 2) Ongoing drug treatment that has not been stabilized for at least 3 months 3) Known current thyroid gastrointestinal or hepatobiliary disease(including liver transaminasesmorethanequalto3ULN) and any muscular disorders (even subclinicalincluding serum CPKmorethanequal to 3ULN) 4)Current or previous alcohol abuse5)Pregnancy and breastfeeding 6) Known previous intolerance to RYR

Design outcomes

Primary

MeasureTime frame
Reduction of LDL-C and LipidsTimepoint: up to 12 weeks

Secondary

MeasureTime frame
Change in clinical symptomsTimepoint: up to 12 weeks

Countries

India

Contacts

Public ContactDr Dipak Ranjan Das

Dabur Research and Development Centre Dabur India limited

baidyanath.mishra@dabur.com911203378606

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Jun 11, 2026