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Homeopathic treatment of high blood pressure

Efficacy of Individualized Homeopathic Medicines in Intervening the Progression of Pre-hypertension to Hypertension: A Double-Blind, Randomized, Placebo controlled Trial

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2018/10/016026
Enrollment
92
Registered
2018-10-15
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

Health Condition 1: R030- Elevated blood-pressure reading, without diagnosis of hypertension

Interventions

Intervention1: Homeopathic individualised medicines in centesimal potency: Intervention is planned as administering indicated homoeopathic medicines in centesimal potencies, as decided appropriate to
dosage and repetition depending upon the individual requirement of the cases. This arm will also receive standardized LSM guidelines. Duration of therapy: 3 months.

Sponsors

DNDe Homoeopathic Medical College and Hospital
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: a) Adults of both sexes b) Age between 18-65 yrs c) Newly diagnosed subjects with prehypertension (JNC-8 classification) (systolic BP [SBP] 120-139 mm Hg and diastolic BP [DBP] 80-89 mm Hg) and of less than one year duration (ICD R03.0) d) New pre-hypertensive patients (those who are accidentally discovered as pre-hypertensives while complaining of some other functional disorders)

Exclusion criteria

Exclusion criteria: a) Body mass index (BMI) more than 35 kg/m2 b) Pregnant and lactating women c) Pre-existing chronic debilitating illness d) Subjects on hormonal contraceptives, steroids or Non steroidal anti-inflammatory Drugs (NSAIDs) e) Any uncontrolled systemic illness, psychiatric diseases and life threatening illness f) Self reported immune-compromised patient g) Undergoing homeopathic treatment for any chronic disease within last 6 months. h) Unwilling to take part or not giving consent to join the study i) Unable to read patient information sheet

Design outcomes

Primary

MeasureTime frame
Systolic and diastolic blood pressureTimepoint: At baseline and every month up to 3 months

Secondary

MeasureTime frame
Measure Yourself Medical Outcome Profile - 2Timepoint: At baseline and every month up to 3 months

Countries

India

Contacts

Public ContactSubhasish Ganguly

D.N.De Homoeopathic Medical College and Hospital

ganguly.subhasish@rediffmail.com9007263548

Outcome results

None listed

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