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To evaluate the efficacy of test product, in terms of reduction in itching, in patients having cutaneous mycosis.

AN OPEN LABEL, PROSPECTIVE REAL-WORLD, POST MARKETING STUDY TO EVALUATE THE EFFECTIVENESS OF LUCRUSH (LULICONAZOLE 1% W/W CREAM) IN PATIENTS OF CUTANEOUS MYCOSIS.

Status
Active, not recruiting
Phases
Phase 4
Study type
Observational
Source
CTRI
Registry ID
CTRI/2021/06/034498
Enrollment
35
Registered
2021-06-30
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

Health Condition 1: B369- Superficial mycosis, unspecified

Interventions

Intervention1: LUCRUSH (LULICONAZOLE 1% W/W CREAM): Thin film to be applied on the affected area and some of the surrounding skin. Gently rub in as directed once a day. One time application

Sponsors

Dr Reddys Laboratories Ltd
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Clinically Diagnosed patients with cutaneous mycosis who are prescribed LUCRUSH as per physicianâ??s discretion

Exclusion criteria

Exclusion criteria: Investigatorâ??s discretion to not to include patients such as of Patients requiring systemic antifungal drugs, pregnant or lactating women, or patients with any significant medical illness such as diabetes, immunocompromised conditions, and other sexually transmitted diseases, etc. Hypersensitivity to Luliconazole based formulation Multiple topical antifungal usage Topical steroid based formulation usage Oral antihistamine usage.

Design outcomes

Primary

MeasureTime frame
Change in itch severity as assessed on 10-point VASTimepoint: 2 min, 5 min, 10 min, 1 hour, 4-hour, 8-hour

Secondary

MeasureTime frame
Number & Type of adverse events during treatment with LucrushTimepoint: 2 min, 5 min, 10 min, 1 hour, 4-hour, 8-hour;Number of patients achieved all night relief from itching by self-assessment questionnaire.Timepoint: 2 min, 5 min, 10 min, 1 hour, 4-hour, 8-hour

Countries

India

Contacts

Public ContactAkhila Paspulate

Dr. Reddys Laboratories Ltd.

anuputtampetare@drreddys.com9892315663

Outcome results

None listed

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