Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-24 @ 11:31 PM
Ignite Modification Date:
2025-12-24 @ 11:31 PM
NCT ID:
NCT02267356
Eligibility Criteria:
Key Inclusion Criteria:
Distal subungual onychomycosis of the great toenail, affecting at least ≥25 to ≤75% of nail.
Positive culture for dermatophytes and positive KOH.
Nail ≤ 3 mm thick at the distal end.
At least ≥ 2 mm of the proximal end of the great toenail must be free of infection.
Subjects must be able to swallow tablets.
Women of childbearing potential and males must use acceptable birth control methods throughout the study.
Key Exclusion Criteria:
Presence of subungual hematoma or melanonychia.
Presence of dermatophytoma/nail streaks and severe onychorrhexis.
Significant dystrophy or anatomic abnormalities of the great toenail.
Presence of any other infections of the foot.
Evidence of clinically significant major organ disease.
Poorly controlled diabetes mellitus.
Onychomycosis involving more than 8 toe nails.
Recent use of systemic antifungal therapy.
Recent of any topical antifungal nail therapy.
Recent use of systemic corticosteroid therapy.
Recent use of immunosuppressive medication.
History of prolonged QT intervals.
Known human immunodeficiency virus (HIV) infection.
Known significant renal or hepatic impairment.
Known history of intolerance or hypersensitivity to azole antifungal drugs.
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Maximum Age:
70 Years
Study:
NCT02267356
Study Brief:
Protocol Section:
NCT02267356