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Clinical Trials/CTRI/2026/02/103999
CTRI/2026/02/103999Not yet recruitingPhase 4

A comparative study of topical 1 percent luliconazole cream versus 20 percent salicylic acid peel in the management of pityriasis versicolor

Dr Snehal Navande1 site in 1 country39 target enrollmentStarted: February 24, 2026Last updated:

Trial Snapshot

Phase
Phase 4
Status
Not yet recruiting
Sponsor
Enrollment
39
Locations
1

Study Overview

Brief Summary

Pityriasis versicolor is a common superficial fungal infection caused by Malassezia species, characterized by hypopigmented or hyperpigmented scaly patches over the trunk and proximal extremities. Topical antifungals remain the mainstay of treatment; however, recurrence and incomplete clearance are frequent.

This prospective, comparative interventional study aims to evaluate and compare the clinical and mycological efficacy of topical 1% luliconazole versus topical 20% salicylic acid peel in patients with pityriasis versicolor involving the body. Eligible patients will be allocated into two treatment groups and followed up at predefined intervals.

Clinical assessment will be done using a standardized clinical severity scoring system, and mycological assessment will be performed using potassium hydroxide (KOH) mount examination. The primary outcome will be mycological clearance, defined as negative KOH mount at the end of treatment.

The study is expected to provide evidence regarding the comparative effectiveness and safety of these commonly used topical treatment modalities in the management of pityriasis versicolor.

Study Design

Study Type
Interventional

Eligibility Criteria

Ages
18.00 Year(s) to 80.00 Year(s) (—)
Sex
All

Inclusion Criteria

  • All patients coming to dermatology OPD with lesions of pityriasis versicolor.

Exclusion Criteria

  • 1 Children below the age of 12 years 2 Any previous history of topical application or previous treatment taken 3 Pregnant and lactating female 4 Patients on any systemic and topical antifungal treatment.

Investigators

Sponsor
Dr Snehal Navande
Sponsor Class
Other [self]
Responsible Party
Principal Investigator
Principal Investigator

Dr Sarah Rehan Hawai

MIMER Medical College and Dr BSTR Hospital Talegaon Dabhade Pune

Study Sites (1)

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