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Exploring Baryta Muriatica 3x For Lowering Cholesterol Levels:A Study On Hyperlipidemia Managment

To Study The Efficacy Of Baryta Muriatica 3x In The Management Of Hyperlipidemia -A Randomized Comparative Clinical Study - NIL

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/11/076703
Enrollment
52
Registered
2024-11-12
Start date
Unknown
Completion date
Unknown
Last updated
2024-12-09

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

Intervention1: BARYTA MURIATICA 3X: Potenstised homoeopathic medicine Baryta Muriatica in the form of pills Dose: 2 tablets thrice a day before meal to be prescribed .With the follow up in each 15 da

Sponsors

Dr Bbi Ameena Mysore
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Case fulfilling the case definition will be included in the study 2. Patient of all genders will be included 3. patients of age group 25-70 years will be included 4. Cases that include lipid profile abnormality i.e; LDL- Cholesterol above 100mg/dL. 5. ACC/AHA CV RISK CALCULATOR with the range of =7.5% risk

Exclusion criteria

Exclusion criteria: 1.Patients with LDL- Cholesterol above 190mg/dL. 2.Patients with Diabetes Mellitus and are on insulin tretament. 3. Patients with severe cardiac illness, chronic kidney diseases, HTN of grade 2,3. 4. Patients who need emergency medical interventions 5.Acute cases will not be taken during the study

Design outcomes

Primary

MeasureTime frame
To assess the effect of Baryta Muriatica 3X on reducing Cholesterol level by evaluating its effect on Low density Lipoprotein(LDL-C)Timepoint: The follow ups will be taken after 15 days and will be assessing the effect of Baryta Muriatica 3X

Secondary

MeasureTime frame
To assess the effect of Baryta Muriatica 3X on newly diagnosed cases of Hyperlipidemia with Primary Hypertension under the age criteria for 25-70 yearsTimepoint: The follow ups will be of 15 days & will be assess the effect of Baryta Muriatica 3X

Countries

India

Contacts

Public ContactDr Bibi Ameena Mysore

Bharati Vidyapeeth (Deemed To Be University) Homoeopathic Medical College And Pune

vishali.dolas@bharatividyapeeth.edu8329474808

Outcome results

None listed

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