Skip to content

Effects of homeopathic medicines on blood lipid profile in adults

A double-blind, randomized placebo-controlled trial of individualized homeopathic medicines in the treatment of dyslipidaemia in adults - nil

Status
Recruiting
Phases
Phase 2Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/08/093315
Enrollment
100
Registered
2025-08-20
Start date
Unknown
Completion date
Unknown
Last updated
2025-09-15

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

Conditions

Health Condition 1: E78- Disorders of lipoprotein metabolism and other lipidemias

Interventions

Intervention1: Individualized homeopathic medicines plus concomitant care: Using centesimal potencies (CH) of approved homoeopathic medications is the intended intervention. The quantity and frequenc

Sponsors

D. N. De Homoeopathic Medical College and Hospital
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Patient suffering from newly diagnosed cases of dyslipidaemia with LDL-C levels of 100-189mg/dl 2. Framingham risk score less than 20% 3. Age between 18 and 65 years. 4. Participants of either sex or transgender.

Exclusion criteria

Exclusion criteria: 1. Patients not providing with written informed consent of participation. 2. Familial hypertriglyceridemia. 3. Person already taking lipid lowering agents. 4. History of myocardial infarction, stenting, coronary artery bypass surgery or stroke. 5. Pregnant, puerperal, and lactating women. 6. Non ambulatory patients 7. Undergoing homoeopathic treatment for any chronic disease within the last 6 months 8. Vulnerable population: Unconscious, non-ambulatory, too sick for consultation, differently abled, terminally ill or critically ill patients, diagnosed cases of unstable mental or psychiatric illness and self-reported immune-compromised state. 9. Uncontrolled hypertension, uncontrolled diabetes, nephritic syndrome, renal insufficiency, uncontrolled hypothyroidism, severe or active liver diseases or any other uncontrolled systemic diseases affecting the quality of life or organ failure. 10. Habits of tobacco chewing and/or smoking, alcoholism, and/or any other form(s) of substance abuse and/or dependence (TAPS tool) 11. Simultaneous participation in any other clinical trials.

Design outcomes

Primary

MeasureTime frame
Blood LDL cholesterol level (LDL-C)Timepoint: At baseline, and after 3 months

Secondary

MeasureTime frame
total cholesterol (TC),Triglycerides(TGs),HDL,VLDL,FBS,PPBS and liver enzymes (AST and ALT)Timepoint: At baseline, and after 3 months;Short form 12(SF-12) health survey questionnaireTimepoint: At baseline, monthly, up to 3 months

Countries

India

Contacts

Public ContactVeena Prakash Bharti

D. N. De Homoeopathic Medical College and Hospital

greeshmarajkp95@gmail.com9745873194

Outcome results

None listed

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