CompletedPhase 4

Ketoconazole Foam 2% for the Treatment of Versicolor

United States11 participantsStarted 2008-11

Plain-language summary

Ten adult patients age 19 and older with a clinical diagnosis of tinea versicolor, as well as a positive Potassium Hydroxide (KOH) using calcofluor. Ketoconazole 2% foam will be used to determine its effectiveness, safety and satisfaction when used to treat tinea versicolor.

Who can participate

Age range

19 Years

Sex

ALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion criteria

. Male or female patients, aged 19 years and over.
. Clinical presentation of tinea versicolor.
. Positive KOH using calcofluor.
. The ability to provide informed consent (including photography release)

Exclusion criteria

. Use of topical antifungal to the affected area in the past 30 days
. Use of topical steroid to the affected area in the past 14 days
. If female, positive urine pregnancy test at screening (female patients of childbearing potential must be practicing a reliable method of birth control, not be planning a pregnancy, not be breast-feeding during the study)
. Patients with a dermatologic condition in the region of the treatment site that in the investigator's opinion may interfere with the study results
. Current diagnosis of immunocompromising conditions
. Any medical or psychiatric condition that may interfere with treatment or compliance

Questions worth asking your doctor

Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.

1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?

Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.

Questions for the trial coordinator

The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.

1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?

A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.

What they're measuring

The Effect of Ketoconazole 2% Foam for the Treatment of Tinea Versicolor

Timeframe: 4 weeks

Trial details

NCT IDNCT00830388

SponsorBoni Elewski, MD

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2010-08

Results submitted2012-05-01

View on ClinicalTrials.gov More Tinea Versicolor trials