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Completed

NCT Number: NCT03130738

Dose-Ranging Study for Miconazole Oil for Treatment of Otomycosis

The purpose of the study is to evaluate the efficacy and safety of active treatment (miconazole oil) for 7 versus 14 days, and to compare 14 days of active treatment (miconazole oil) to inactive treatment (placebo) over a 14-day treatment duration, in subjects with fungal infection (otomycosis) of the external ear.

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Key information

Age range

25 month and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

Head and Neck Surgery Specialist, Chula Vista, California, United States

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About this study

Miconazole, an imidazole antifungal agent, is commonly used for different types of fungal skin infections, such as Candida, ringworm, jock itch, athlete's foot, nail fungus, vaginal yeast infections, and oropharyngeal candidiasis. The 2% formulation of miconazole is commonly used for dermatophytic infections. The mechanisms of action of miconazole against fungi in general appear to be applicable to fungi associated with otomycosis, in that miconazole has been demonstrated to have activity in vitro against some clinical isolates of fungi associated with human otomycosis in the US.

Miconazole targets the cytochrome P450-dependent enzyme 14-α-sterol demethylase, an enzyme that is also involved in mammalian cholesterol synthesis, resulting in inhibition of ergosterol biosynthesis in the cell membrane of the fungal organism. Because ergosterol is an important component of the cell membrane, inhibition of its synthesis inhibits fungal cell growth.

In addition to its activity toward the enzyme 14-α-sterol demethylase, miconazole also leads to increased reactive oxygen species in fungal organisms, which appears to result in fungicidal activity.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Uncomplicated otomycosis of the external ear only, age more than 2 year

Exclusion criteria

  • Pregnancy
  • Other dermatoses or conditions of the ear that may interfere with the evaluation of otomycosis, including concomitant otic infections (including bacterial infection) that require antimicrobial treatment, disease that has spread beyond the external ear(s), or pre-existing skin atrophy of the affected ear(s)
  • Tympanostomy tube or perforated tympanic membrane in the ear(s) that will be treated
  • Previous surgery affecting the ear(s) that will be treated, except for prior tympanostomy tube(s) that had been removed and had completely healed
  • Previous use of medicated treatments for otomycosis or participation in another investigational study within 28 days of study entry
  • Previous use of any systemic antifungal therapy, warfarin, and immunosuppressive or immune-stimulating drugs within 28 days of study entry, or systemic steroids within 3 months of study entry
  • Recurrent otomycosis that had been unresponsive to previous antifungal treatment
  • Known hypersensitivity to any of the components in the test formulation

Treatment and study plan

7-Day Miconazole Oil (Miconazole 2%)

Drug

7 days of 2x per day treatment with Miconazole Oil (Active Drug Product 2% Miconazole)

Other names: Miconazole

14-Day Miconazole Oil (Miconazole 2%)

Drug

14 days of 2x per day treatment with Miconazole Oil (Active Drug Product 2% Miconazole)

Other names: Miconazole

14-Day Placebo - Oil Vehicle

Drug

14 days of 2x per day treatment with Placebo - Oil Vehicle, Study Drug base without active ingredient

Other names: (Miconazole) Placebo Oil Vehicle

Primary outcomes

  1. Primary Efficacy Endpoint

    Time frame: At Test of Cure visit (Day 15 for 7 Day Active and Day 22 for 14 Day Active and 14 Day Vehicle)

    Percentage of subjects in MITT population, at the "Test of Cure" visit with "Therapeutic cure", defined as a negative fungal culture plus "clinical cure" defined as the absence of all otomycosis signs and symptoms for pruritus, debris, fungal elements, and pain.

Secondary outcomes

  1. Secondary Efficacy Endpoints

    Time frame: At Test of Cure visit (Day 15 for 7 Day Active and Day 22 for 14 Day Active and 14 Day Vehicle)

    • Percentage of subjects in MITT population with clinical cure at the Test of Cure Visit
    • Percentage of subjects in MITT population with a negative fungal culture at the Test of Cure Visit
    • Percentage of subjects in MITT population with a negative fungal culture at the Test of Cure visit as well as individual sign or symptom score of 0 or 1 on each of the scales for pruritus and debris and a score of 0 on each of the scales for fungal elements and pain (Secondary therapeutic cure).
    • Percentage of subjects in MITT population with individual signs or symptoms with a score of 0 or 1 on each of the scales for pruritus and debris and a score of 0 on each of the scales for fungal elements and pain (Secondary clinical cure).

Sponsors and collaborators

Lead sponsor

Hill Dermaceuticals, Inc.

Industry

Collaborators

  • QST Consultations, Ltd.

Registry information

Official study title

Dose-Ranging Study of the Efficacy and Safety of Miconazole Oil Used for 7 or 14 Days Compared With Vehicle in the Treatment of Otomycosis

Important dates

Study start
2017
Primary completion
2019
Study completion
2019
First posted
Apr 26, 2017
Registry last updated
Oct 5, 2022

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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