Systemic Uptake of Diclofenac Sodium in Combination With Miconazole as Antifungal Nail Gel When Applied Daily With Monitoring of Hepatic and Renal Enzymes, and Serum Levels of Diclofenac 12 Hours After Application, and at 3 and 6 Months Study

Status unconfirmed · Phase 2

Conditions studied: Tinea Unguium, Onychomycosis

In brief

Study evaluates these take of diclofenac sodium when used in conjunction with miconazole and urea as a topical antifungal nail gel treatment for onychomycosis. All of the patient's will be treated with the active formula and blood levels of diclofenac sodium tested for as well as monitoring of hepatic and renal functions

Key facts

Study ID

NCT04341402

Run by

William N Handelman

People needed

30

Starts

2020-05-01

Expected to finish

2021-05-01

Last updated by the study team

2020-04-10

Who can join

Age: 21 and older, up to 100. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Male or female ≥ 21 years of age at Visit 1.
• Not pregnant.
• Stage 3 or lower Chronic Renal Failure.
• PT/INR < 1.3 and not on anti-thrombotic; AST, ALT, Total Bilirubin WNL.
• Documentation of a diagnosis of tinea unguium as evidenced by one or more clinical features consistent with the onychomycosis and one or more of the following criteria: KOH prep of the nail scrapings or positive culture of the nail scrapings; culture of nail with growth of any of the following Dermatophytes, non-dermatophytes or yeast.
• TABLE 1 Epidermophyton floccosum Trichophyton mentagrophytes Trichophyton rubrum Acremonium Alternaria species Aspergillus species Botryodiplodia theobromae Fusarium species Onycochola canadensis Pyrenochaeta unguis-hominis Scytalidium dimidiatum scopulariopsis species Scytalidium hyalimum Candida albicans

You may not qualify if…

• Chronic renal failure, chronic liver disease, alcoholism, pregnant, breastfeeding, or unwilling to practice birth control during participation in the study if of childbearing age..
• Presence of a condition or abnormality that in the opinion of the Investigator would compromise the safety of the patient or the quality of the data.
• Concomitant use of any prescribed medication that may be adversely affected by diclofenac sodium.

Where it is running

• Bay Area Medical — St. Petersburg, Florida, United States (enrolling)

Full record on ClinicalTrials.gov

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