Comparative Study Between Pulsed and Continuous Itraconazole for the Treatment of Onychomycosis
Sponsored by Combined Military Hospital Abbottabad
About this trial
Last updated 3 years ago
Study ID
Status
Type
Phase
Placebo
Accepting
Not accepting
Trial Timing
Ended 4 years ago
What is this trial about?
What are the participation requirements?
Inclusion Criteria
- Patients age between 20-60 years
- Patients positive for fungus via direct microscopy due to the identification of hyphae or blastospores on the target toenail
- Patients positive fungal culture. Patients who had not applied any topical agent to the target toenail for the last 1 month
Exclusion Criteria
- Pregnant patients
- Patients with poor adherence
- Lactating women.
- Patients previously allergic to oral itraconazole.
- Patients with elevated baseline liver function tests such as ALT, AST, alkaline phosphatase, and total bilirubin twice the upper limit of normal
- History of renal disease.
- Patients unresponsive to systemic antifungal therapy within the past year
- History of using systemic immunosuppressants.
- Patients exhibiting evidence of ventricular dysfunction and history of congestive heart disease
- Immunocompromised patients