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Evaluation of fractional laser and topical antifungal effectiveness versus systemic antifungal to improve onychomycosis

Phase 2
Conditions
onychomycosis.
Tinea unguium
Registration Number
IRCT2016022925539N6
Lead Sponsor
Vice chancellor for research , Iran University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
54
Inclusion Criteria

Onychomycosis Infection ; lack of topical or oral drug allergy
Exclusion criteria: Absence of follow up by patients and Lack of consent for treatment; Complications such as allergy to topical or oral agent

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Fungal nail infection. Timepoint: 0, 1 and 2 months during treatment . And 3 and 6 months after treatment. Method of measurement: The involvement of the nail plate with standard photography.
Secondary Outcome Measures
NameTimeMethod
Response to treatment According to the patient. Timepoint: After completion of treatment. Method of measurement: The percentage and score of the patient to treatment (0 to 100%).;Satisfaction amount. Timepoint: After completion of treatment. Method of measurement: Comparison of reduction nail involvement by patient , before and after treatment According to schedule (score 0 to 10).
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