AI Article Synopsis

  • A clinical trial compared the effectiveness of 2% fenticonazole cream versus 1% bifonazole cream on 41 patients with dermatomycosis, with assessments at multiple time points throughout treatment.
  • Both creams were found to be effective, but fenticonazole showed superior results, curing 15 out of 21 patients compared to 7 out of 20 for bifonazole after 3 weeks, a statistically significant difference (p = 0.021).
  • No adverse effects were recorded for either treatment, and all patients had no recurrence of disease after treatment follow-up.

Article Abstract

A randomized, double-blind clinical trial was undertaken in 41 patients with dermatomycosis to compare topical 2% fenticonazole cream (group A: 21 patients) with topical 1% bifonazole cream (group B: 20 patients). Treatment was performed as a once daily application. Mycological and clinical parameters were assessed before treatment and after 7, 14, 21 and 28 days. At the control visits the clinical investigator also expressed an overall judgement on the patient's state of disease. This parameter was based on a combined clinical and mycological assessment by the physician; laboratory screening investigations were undertaken before and at the end of treatments. All patients were checked for their state of disease 3-4 weeks after the end of treatment. All assessment criteria showed fenticonazole to be at least as efficacious as bifonazole. Several trends in favor of fenticonazole were also found: fenticonazole achieved superior results in the overall clinical evaluation, and after 3 weeks of treatment 15 patients out of 21 on fenticonazole were cured in mycological and clinical terms, whereas treatment with bifonazole resulted in complete healing of only 7 patients out of 20. This difference is statistically significant (p = 0.021) and indicates a more rapid therapeutic activity of fenticonazole. At the posttreatment rechecks no recurrent disease was registered, irrespective of whether patients had received fenticonazole or bifonazole. Laboratory screening investigations revealed no evidence of significant treatment-related changes or abnormalities in both treatments. No adverse events were noted for either treatment.

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Source
http://dx.doi.org/10.1159/000248524DOI Listing

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