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Clinical signs and symptoms, microscopic examination of tissue changes and Colour changes in Lichen Planus Pigmentosus in a tertiary care hospital

Clinicopathological, Dermoscopic and Colorimetric analysis in Lichen Planus Pigmentosus in a tertiary care hospital: A cross-sectional study - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2023/11/059870
Enrollment
60
Registered
2023-11-15
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: L438- Other lichen planus

Interventions

Intervention1: NIL: NIL

Sponsors

Dr Youvalakshmi S
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients with clinical and histopathological features of lichen planus pigmentosus will be included in this study.

Exclusion criteria

Exclusion criteria: Any contraindications to biopsy like bleeding disorders will be excluded from this study

Design outcomes

Primary

MeasureTime frame
To study the clinicopathological and dermoscopic features of lichen planus pigmentosus. To quantify the intensity of pigmentation in lichen planus pigmentosus by colorimetric analysis Timepoint: 1 week to 2 weeks—

Secondary

MeasureTime frame
To quantify the intensity of pigmentation in lichen planus pigmentosus by colorimetric analysis Timepoint: 1 week to 2 weeks—

Countries

India

Contacts

Public ContactDr Youvalakshmi S

Sri Manakula Vinayagar Medical College and Hospital

karthikderm@gmail.com9787971430

Outcome results

None listed

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