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Study of homoeopathic medicine Nerium Oleander in cases of eczema using scale (scorad index)

A CLINICAL STUDY ON THE EFFICACY OF HOMEOPATHIC MEDICINE NERIUM OLEANDER IN THE TREATMENT OF ATOPIC DERMATITIS USING SCORAD INDEX - NEO-AD Study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/09/095054
Enrollment
50
Registered
2025-09-18
Start date
Unknown
Completion date
Unknown
Last updated
2025-10-13

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

Conditions

Health Condition 1: L209- Atopic dermatitis, unspecified

Interventions

Intervention1: Nerium Oleander: Selection Of Potency Will Be Based On Totality Of Symptoms And Susceptibility Of Patient And The Case Will Be Reviewed Every 7 And 15 Days Depending Upon The Requiremen

Sponsors

Dr Sonal Yogendra Tiwari
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: i.Patients diagnosed with Atopic Dermatitis as per Hanifin and Rajka criteria and serum IgE levels. ii.Patients of age groups from 18 to 60 years. iii.Patient whose SCORAD index would be mild to moderate in terms of severity. iv.Patients who have not taken any antihistamines or corticosteroids for at least 7 days prior to the start of treatment. v.Patients willing to give informed consent and comply with the study protocol.

Exclusion criteria

Exclusion criteria: i.Patients with suffering from secondary infection like presence of infected eczema, impetigo, eczema herpeticum, or other acute bacterial and viral skin infections. ii.Patients with age less than 18 years and more than 60 years. iii.Patients with severe SCORAD scored disease should not be considered. iv.Patients who have taken any antihistamine or corticosteroid for at least 7 days prior to treatment with homoeopathic medicine. v.Patients with other dermatological conditions co-existing chronic skin diseases like psoriasis, seborrheic dermatitis, contact dermatitis, etc., that may interfere with diagnosis or outcome. vi.Patients with immunocompromised status, autoimmune diseases, or systemic infections. vii.Pregnant or lactating women ,unless ethically approved and monitored. viii.Patients who are unable or unwilling to comply with the study protocol, such as adhering to treatment regimen and attending follow-up visits

Design outcomes

Primary

MeasureTime frame
Mean change in SCORAD Index (Scoring Atopic Dermatitis Index) score from baseline to end of treatment.Timepoint: 00-03 months for enrollment of cases

Secondary

MeasureTime frame
Change in Visual Analogue Scale VAS for pruritus and sleep loss. Timepoint: 3rd , 6th , 9th months;Proportion of participants achieving equal to or more than 50 percentage reduction in SCORAD index scoreTimepoint: 3rd,6th,9th month

Countries

India

Contacts

Public ContactDr Bankim A Patel

Anand Homoeopathic Medical College And Research Institute,Anand

pramukh.homeo@gmail.com9428066383

Outcome results

None listed

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