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Role of Homoeopathic Medicines in treatment of Vitiligo

Effectiveness of individualized homoeopathic medicines vs Arsenicum Sulphuricum Flavum in improving the quality of life among vitiligo patients: An open label randomised controlled clinical trial - NIL

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/12/077819
Enrollment
60
Registered
2024-12-09
Start date
Unknown
Completion date
Unknown
Last updated
2025-02-03

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

Conditions

Health Condition 1: L80- Vitiligo

Interventions

Intervention1: Arsenicum Sulphuricum Flavum: Started with 6c potency in each case. Route of drug administration - oral. Repetition of dosages will be done on the basis of requirement of case as per t

Sponsors

Dr Ankita Jain
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.Patient suffering from vitiligo. 2.Both sexes of age group 5 years to 65 years. 3.Patient willing to give voluntary written informed assent and consent (greater than 18 years).

Exclusion criteria

Exclusion criteria: 1.Vitiligo patients suffering from any life-threatening illness who are terminally ill, under immuno-suppressive treatment or self-reported immuno-compromised state. 2.Patients of malignancy or too sick for consultation. 3.Diagnosed case of mental illness / psychiatric/ other uncontrolled/ life threatening illness affecting quality of life/any organ failure. 4.Pregnant ladies are excluded. 5.Unwilling to take part and not giving consent to join the study. Patients unable to comply with the study protocol. Substance abuse and or dependence.

Design outcomes

Primary

MeasureTime frame
It is expected that there will be repigmentation in depigmented area of skin with the individualized homoeopathic medicines compared to Arsenicum Sulphuricum Flavum in vitiligo.Timepoint: At baseline (0 weeks) and after 9 months(36 weeks)

Secondary

MeasureTime frame
It is expected that there will be improvement in patient’s outcome and general well being, without any substantial medicinal adverse effects hence an improvement in quality of life (DLQI) & significant reduction in VASI scores and Re-pigmentation on hypopigmented/ depigmented patches.Timepoint: At baseline (0 weeks) and after 9 months (36 weeks)

Countries

India

Contacts

Public ContactDr Ankita Jain

Dr B R Sur Homoeopathic Medical College Hospital And Research Centre, Nanakpura Motibagh

neenamehan@gmail.com9811578570

Outcome results

None listed

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