The effect of fluconazole lozenge on oral candidiasis
Phase 3
Recruiting
- Conditions
- Oral candidiasis.Candidal stomatitisB37.0
- Registration Number
- IRCT20191106045356N16
- Lead Sponsor
- Yazd University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 50
Inclusion Criteria
The patient is undergoing cancer chemotherapy in Yazd hospitals.
The woman should not be pregnant or lactating.
Willingness to participate in the study and complete the informed consent form
Age 18 to 70 years
Exclusion Criteria
The occurrence of an allergic reaction to fluconazole
Aggravation of the disease and the need for drug intervention to control the disease
Non-cooperation in the use of medication
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Total area of oral candidiasis lesions. Timepoint: At the beginning of the treatment and after every 2 days until 10 days, the condition of oral candidiasis lesions is evaluated in terms of the total area of the lesions. Method of measurement: Determining the total area of oral candidiasis lesions through Fiji software.
- Secondary Outcome Measures
Name Time Method Cotton feeling in the mouth. Timepoint: the beginning of the treatment and after every 2 days up to 10 days, the condition of oral candidiasis lesions is evaluated in terms of the feeling of cotton in the mouth (score 0 to 4). Method of measurement: Scoring the feeling of cotton in the mouth using a questionnaire.;Decreased taste. Timepoint: At the beginning of treatment and after every 2 days until 10 days, the condition of oral candidiasis lesions is evaluated in terms of taste loss (score 0 to 4). Method of measurement: Scoring of taste reduction using a questionnaire.