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serum chemokines levels in vitiligo and correlation with dermoscopic findings and severity of disease.

SERUM CXCL10 LEVELS IN NON-SEGMENTAL VITILIGO AND ITS CORRELATION WITH DERMOSCOPIC FINDINGS AND DISEASE SEVERITY: A CROSS-SECTIONAL STUDY - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2023/11/060132
Enrollment
120
Registered
2023-11-22
Start date
Unknown
Completion date
Unknown
Last updated
2023-12-19

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

None listed

Sponsors

Department of Dermatology, Venereology and Leprosy, Government Medical College, Srinagar
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Age group 12-65 years. Age and sex matched apparently healthy controls. Patients with non-segmental vitiligo. Both males and females will be included.

Exclusion criteria

Exclusion criteria: Patients receiving systemic treatment in the last 3 months. Patients receiving narrow band phototherapy (NB UVB). Patients with any autoimmune disorder such as rheumatoid arthritis, inflammatory bowel disease, psoriasis, systemic lupus erythematosus, patients with type 1 and 2 diabetes mellitus and thyroid disease.

Design outcomes

Primary

MeasureTime frame
Estimation of Serum levels of CXCL10 in patients and controls.Timepoint: Estimation of Serum CXCL10 Levels, use of dermoscopy in detection of vitiligo activity and stability, vitiligo disease activity score (VIDA),at baseline.Patients will be followed up every 4 weeks, for 16 weeks. At each follow up,VIDA Score and dermoscopy will be done.

Secondary

MeasureTime frame
1.Estimation of serum CXCL10 Levels in patients & controls 2.VIDA SCORE 3.VASI SCORE 4.Dermoscopic Examination of vitiligo to assess the activity of disease.Timepoint: Estimation of Serum CXCL10 Levels, use of dermoscopy in detection of vitiligo activity & stability, vitiligo disease activity score (VIDA),at baseline.Patients will be followed up every 4 weeks, for 16 weeks. At each follow up,VIDA Score & dermoscopy will be done.

Countries

India

Contacts

Public ContactDr Ishrat binti ismail

Department of Dermatology, Venereology and Leprosy, Government Medical College, Srinagar

yasmeenasif76@gmail.com9419040771

Outcome results

None listed

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