Oral candidiasis. Candidal stomatitis
Conditions
Interventions
Intervention 1: Intervention group: Including 25 patients hospitalized in Yazd hospitals and undergoing cancer chemotherapy, who were diagnosed with oral candidiasis and met the inclusion criteria, an
Sponsors
Yazd University of Medical Sciences
Eligibility
Sex/Gender
All
Age
18 Years to 70 Years
Inclusion criteria
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
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
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 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
| Measure | Time frame |
|---|---|
| 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. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactDr. Mohsen Zabihi
Yazd University of Medical Sciences
Outcome results
None listed