Skip to content

Psoriasis vulgaris and Homoeopathy

Efficacy of Individualized Homoeopathic Intervention to Evaluate the Response in the selective inflammatory biomarkers (CBC, ESR, hS-CRP, IL-6) in Psoriasis vulgaris- Randomized, Double-Blind, Placebo-Controlled Cross-Over Trial - NA

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/02/080126
Enrollment
104
Registered
2025-02-07
Start date
Unknown
Completion date
Unknown
Last updated
2025-03-03

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

Conditions

Health Condition 1: L400- Psoriasis vulgaris

Interventions

Intervention1: Individualized Homoeopathic medicines will be remedies that will be prescribed and administered orally in centesimal potencies (6c, 30c, 200c, 1M, 10M, and 50M) with necessary repetitio

Sponsors

National Homoeopathy Research institute in Mental health Kottayam Kerala India
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Age between 18- 60 years, all genders. Clinically diagnosed with a mild, moderate case of psoriasis vulgaris ( according to the classification of psoriasis severity) with increased IL-6biomarker.

Exclusion criteria

Exclusion criteria: Pregnant and lactating mothers Severe form of psoriasis vulgaris ( according to the classification of psoriasis Severity ) Cases with psoriatic arthritis. Evidence of skin conditions other than psoriasis that would interfere with evaluations of the effect of study medication on psoriasis Participants are on systemic immune-suppressive therapy or any treatment below six months. The patient has generalized pustular Psoriasis or erythrodermic Psoriasis with Significant functional impairment and high levels of distress.

Design outcomes

Primary

MeasureTime frame
Changes in the IL-6 inflammatory biomarkers baseline after the 6th month and at the 12th month after the intervention in both the verum and placebo groupsTimepoint: Changes in the IL-6 inflammatory biomarkers baseline after the 6th month and at the 12th month after the intervention in both the the verum and placebo groups

Secondary

MeasureTime frame
Changes in the PASI score before and after treatment before and after intervention in both verum and placebo groupsTimepoint: Baselin,Every 3, 6, 9 and 12 months;Changes in the Dermatology Life Quality Index (DLQI) score before and after intervention in both verum and placebo groupsTimepoint: Baseline, Every 3,6,9 and 12 months;Outcome related to impact in daily living (ORIDL) score after intervention in both verum and placebo groupsTimepoint: Every 3,6,9 and 12 months

Countries

India

Contacts

Public ContactDr. Sitharthan.R.

Kerala university of Health Sciences

sitharthanr@gmail.com9443203174

Outcome results

None listed

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