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psoriasis with its psychological origins

A confirmatory study of An Understanding of psychosomatic origin of psoriasis and its homeopathic management with reference to complete repertory and medicine from kali group, calcarea group, sulphur and lycopodium in the Anand City - NIL

Status
Active, not recruiting
Phases
Phase 2Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/06/112480
Enrollment
47
Registered
2026-06-11
Start date
Unknown
Completion date
Unknown
Last updated
2026-06-22

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

Conditions

Health Condition 1: L409- Psoriasis, unspecified

Interventions

Intervention1: Kali group, calcarea group, lycopodium and sulphur: Potency: 6C, 30C, 200C, 1M, LM 0/1, LM 0/2. Repetition: as per the need of patient and observation will be done at every 5th, 7th, an

Sponsors

dr Nirali Modi
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Pre-diagnosed and cases with clinical presentation of Psoriasis were selected randomly. 2. Cases from age 18 to 65 will be included in the study irrespective of gender. 3. Diagnosed cases of Psoriasis which were under treatment by other schools of medicines, but desired to have homoeopathic treatment. 4. Patient with other modern medicine will be observed with decrease in intake of medicine other than homoeopathy and how much of changes are seen on basis of PASI with relation to DCPR. 5. Diagnosis shall be done with PASI score where PASI Score from 0- 40 will be selected. 6. Medicine from Kali Group, Calcarea group, Sulphur and lycopodium will be selected for the research.

Exclusion criteria

Exclusion criteria: 1. Cases with severe systematic disease were excluded. 2. Cases with irreversible pathology except Psoriasis.

Design outcomes

Primary

MeasureTime frame
Change in the Psoriasis Area and Severity Index (PASI) score to the end of the treatment period. A decrease in the PASI score will indicate reduction in disease severity and successful therapeutic intervention.Timepoint: Baseline (Week 0), Mid-treatment (Week 18), and End of treatment (Week 36)

Secondary

MeasureTime frame
NILTimepoint: NIL

Countries

India

Contacts

Public ContactNirali Chirag Modi

dr.v.h.dave homoeopathic medical college

thatsnj@gmail.com09978991391

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Jun 29, 2026