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Blood Protein Levels and Psoriasis Severity

Estimation of serum adenosine deaminase and high sensitivity c ? reactive protein levels in psoriasis vulgaris and their correlation with disease severity. - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2025/08/093885
Enrollment
63
Registered
2025-08-29
Start date
Unknown
Completion date
Unknown
Last updated
2025-09-15

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: Nil: Nil

Sponsors

Indian Association of Dermatologists Venereologists and Leprologists
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Adults aged 18 years or older who are willing to provide informed consent to participate in the study. 2. Individuals with a confirmed diagnosis of psoriasis vulgaris, whether previously diagnosed or newly diagnosed.

Exclusion criteria

Exclusion criteria: 1. Patients with a clinical diagnosis of palmoplantar psoriasis, pustular psoriasis, or erythrodermic psoriasis 2. Patients who are obese (BMI 30 kg/m2 or higher) 3. Patients who have used topical medications in the past 2 weeks, systemic therapy in the past 4 weeks, or biologic therapy in the past 8 weeks 4. Pregnancy or lactation 5. Patients with other existing dermatological conditions, including mycosis fungoides, hidradenitis suppurativa, atopic dermatitis, contact dermatitis, and cutaneous leishmaniasis 6. Patients with a history of systemic infections or active inflammatory conditions, including pneumonia, liver disease, tuberculosis, sarcoidosis, infectious mononucleosis, rheumatoid arthritis, malignancies, and autoimmune connective tissue diseases.

Design outcomes

Primary

MeasureTime frame
To estimate the serum levels of adenosine deaminase and high sensitivity C-reactive protein in individuals diagnosed with psoriasis vulgaris and evaluate their correlation with disease severity.Timepoint: Serum ADA and hs-CRP levels will be estimated after completing data collection from all enrolled patients. Until then, blood samples will be stored under appropriate conditions in the institutional lab. Assay kits will be procured just before analysis, approximately 6 months after sample collection begins.

Secondary

MeasureTime frame
To evaluate the correlation between ADA, hsCRP levels, & the severity of psoriasis vulgaris, as measured by the Psoriasis Area & Severity Index (PASI) score.Timepoint: To evaluate the correlation between ADA, hsCRP levels, & the severity of psoriasis vulgaris, as measured by the Psoriasis Area & Severity Index (PASI) score which will be done after data analysis, approximately 1 year from intitation of sample collection.

Countries

India

Contacts

Public ContactShivashankara AR

Father Muller Medical College Hospital

arshiva72@gmail.com9880146133

Outcome results

None listed

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