Vaginal candidiasis. Candidiasis of vulva and vagina
Conditions
Interventions
Intervention 1: For one week, treated with 3% jujube vaginal cream and 1% clotrimazole, one applicator every night. Intervention 2: Control group: treated with clotrimazole 1% vaginal cream, one appli
Sponsors
Mashhad University of Medical Sciences
Eligibility
Sex/Gender
Female
Age
15 Years to 49 Years
Inclusion criteria
Inclusion criteria: Written consent to participate in the study Have minimum literacy Resident of Mashhad Married and age range 15-49 Absence, no use of special medicine in the last two weeks No allergy to clotrimazole and jujube No pregnancy or breastfeeding No use of IUD and hormonal contraceptive method No recurrent vulvovaginitis candidiasis No use of oral and topical antifungal (vaginal candidiasis treatment) At least a score of 3 from the total score of symptoms of vaginal candidiasis Bell (according to the questionnaire) Positive test answer from the candidate's point of view
Exclusion criteria
Exclusion criteria: Occurrence of pregnancy Forgetting medication more than once Allergy to given medication Use of other antifungals Monthly habit during the study period Intimacy without using condom Withdrawal from participation in the research by the research unit
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Vaginal candidiasis. Timepoint: One week ± 24 hours. Method of measurement: Culture of vaginal secretions in the laboratory. | — |
Secondary
| Measure | Time frame |
|---|---|
| Itching. Timepoint: Before treatment, one week ± 24 hours after treatment. Method of measurement: Patient history.;Erythema. Timepoint: Before treatment, one week ± 24 hours after treatment. Method of measurement: Patient history.;Burning. Timepoint: Before treatment, one week ± 24 hours after treatment. Method of measurement: Patient history.;Dys paranoia. Timepoint: Before treatment, one week ± 24 hours after treatment. Method of measurement: Patient history.;The result of the culture of vaginal secretions. Timepoint: Before treatment, one week ± 24 hours after treatment. Method of measurement: Patient history. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactShima Bahadri
Mashhad University of Medical Sciences
Outcome results
None listed