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Homoeopathic medicines for Acne vulgaris

THE EFFECT OF INDIVIDUALIZED HOMOEOPATHIC MEDICINES IN CENTESIMAL POTENCY IN COMPARISON WITH 50-MILLESIMAL POTENCY FOR THE TREATMENT OF PATIENTS HAVING ACNE VULGARIS: AN OPEN LABEL, RANDOMIZED DOUBLE-ARM STUDY - Nil

Status
Active, not recruiting
Phases
Phase 2Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/03/082231
Enrollment
90
Registered
2025-03-12
Start date
Unknown
Completion date
Unknown
Last updated
2025-04-07

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

Conditions

Health Condition 1: L700- Acne vulgaris

Interventions

Intervention1: Individual Homoeopathic Medicine in Centesimal Potency: Intervention is planned as administering indicated homoeopathic remedies in centesimal potency. Each dose consisted of 1 cane sug
dosage and repetition depending upon the individual requirement of the cases. All medicines will be procured from a Good Manufacturing Practice (GMP)-certified firm. Intervention2: Individual Homoeopa

Sponsors

THE CALCUTTA HOMOEOPATHIC MEDICAL COLLEGE AND HOSPITAL
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. All the patients clinically diagnosed as having Acne vulgaris [ICD11 code: ED80] characterised by comedones papules, pastules, nodules on face and trunk. 2. Age 10 to 50 years. 3. Both sexes and transgenders. 4. Patients giving written informed consent (for ages 18 to 50 years)/assent (for ages 10 to 17 years) to participate. 5. Patients with known but controlled systemic disease.

Exclusion criteria

Exclusion criteria: 1. Patients not giving written informed assent and/or consent to participate. 2. Patients using oil-based cosmetics for 6 months. 3. Patients under hormonal treatments. 4. Co-morbid skin conditions like Psoriasis, Lichen planus, eczema etc. 5. Vulnerable population unconscious, non-ambulatory, too sick for consultation, differently abled, terminally or critically ill patients, mentally incompetent people. 6. Pregnant and puerperal women and lactating mothers. 7. Diagnosed cases of unstable mental or psychiatric illness or other uncontrolled or life-threatening illness affecting quality of life or any organ failure. 8. Substance abuse or dependence. 9. Self-reported immune-compromised state. 10. Undergoing homoeopathic treatment for any chronic disease within the last 6 months. 11. Simultaneous participation in any other clinical trial.

Design outcomes

Primary

MeasureTime frame
Comparing the effects of individualised homoeopathic medicines prescribed in centesimal potency with individualised homoeopathic medicines prescribed in 50-millesimal potency.Timepoint: At the baseline, and every one month up to 3 months.

Secondary

MeasureTime frame
1. Assessment of life quality index. 2. Finding out multifactorial causation.Timepoint: At the baseline, and every one month up to 3 months.

Countries

India

Contacts

Public ContactRajat Chattopadhyay

The Calcutta Homoeopathic Medical College and Hospital

dr.rajatchatterjee@gmail.com9331041142

Outcome results

None listed

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