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Homoeopathic treatment of Psoriasis

Observational study to evaluate response to homoeopathic treatment in psoriasis.

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2018/11/016481
Enrollment
300
Registered
2018-11-30
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: L40- Psoriasis

Interventions

None listed

Sponsors

Central Council for Research in Homoeopathy
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Cases presenting with plaque type psoriasis i.e., well-defined, erythematous, scaly lesion which becomes slivery on attempt to scrape.

Exclusion criteria

Exclusion criteria: 1.Cases with guttate psoriasis & pustular psoriasis. 2.Cases with psoriatic arthritis 3.Not on any treatment for psoriasis over the last 6 months 4.Patents willing to refrain from using any of the following treatments during the study period: o Systemic treatments for psoriasis (e.g., PUVA, cyclosporine, corticosteroids, methotrexate, oral retinoids, MMF, thioguanine, hydroxyurea, sirolimus, azathioprine, 6-MP, etanercept) and immunosuppressive medications for any indication other than psoriasis. o Treatment with UVB phototherapy and all other topical treatments for psoriasis (e.g., topical corticosteroids, calcipotriene, tazarotene, anthralin, tar). Tanning booths or non-prescription UV light sources are not to be used. •Evidence of skin conditions (eg, eczema) other than psoriasis that would interfere with evaluations of the effect of study medication on psoriasis •Be a candidate for systemic immune-suppressive therapy, in the opinion of the investigator, where in the patient has generalized psoriasis with significant functional impairment and high levels of distress.

Design outcomes

Primary

MeasureTime frame
Change in psoriasis severity, which is assessed by grading systems using PASI score. Psoriasis Area and Severity Index (PASI) is an established psoriasis severity assessment tool that will be used as a measure of the effects of homoeopathic treatment in patients of psoriasis at baseline and at monthly intervals for 12 months â?¢Change in participant quality of life score as measured by validated psoriasis specific quality of life scales i.e. Psoriasis Disability Index (PDI). Timepoint: Baseline at 0, monthly follow up at 1,2,3,4,5,6,7,8,9,10,11,12 months

Secondary

MeasureTime frame
Time to next �are measured during the period of follow upTimepoint: at monthly follow up 1,2,3,4,5,6,7,8,9,10,11,12 months

Countries

India

Contacts

Public ContactDr Anil Khurana

Central Council for Research in Homoeopathy

anil23101961@gmail.com01128525749

Outcome results

None listed

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