Evaluation of the effect of Nano zataria multiflra antifungal supplement on patients with onychomycosis with saprophytic agent

Phase 2

Recruiting

• Conditions: onychomycosis.; Tinea unguium; B35.1

• Registration Number: IRCT20210611051539N3
• Lead Sponsor: Mazandaran University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 13 March 2023

Recruitment & Eligibility

• Status: Recruiting
• Sex: All
• Target Recruitment: 30

Inclusion Criteria

All people over 18 years old with mild-moderate onychomycosis caused by filamentous fungi

Exclusion Criteria

Patients who have taken antifungal drugs during treatment

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Improvment of fungal lesions in term of clinical and mycological criteria. Timepoint: before the intervention and 2,4 weeks after the treatment start. Method of measurement: Examining clinical symptoms such as inflammation, itching, scaling and examination in terms of direct smear and fungal culture in the interval of 2, 4 and 6 weeks.