candidiasis vulvovaginit. Vaginitis, vulvitis and vulvovaginitis in diseases classified elsewhere
Conditions
Interventions
Intervention 1: Intervention group: It consists of 30 people, each of whom receives a 2-gram vaginal suppository containing 0.1 cc of Zhumeria maidae essential oil along with clotrimazole suppository
Sponsors
Islamic Azad University
Eligibility
Sex/Gender
Female
Age
18 Years to 50 Years
Inclusion criteria
Inclusion criteria: women aged 18 to 50 years Married lack of sensitivity to the plant compounds of Zhumeria majdae lack of sensitivity to clotrimazole signature the consent form to participate in the study Exclusioncriteria Diagnosis of vaginal candidiasis infection
Exclusion criteria
Exclusion criteria: pregnancy and lactation menopause underlyingdiseases forgetting a dose or more patientunwillingness to continue treatme menstruation during the study abnormal uterine bleeding sensitivity to Zhumeria majdae sensitivity to clotrimazole
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Itching. Timepoint: Start of study - 7 days after the start of the study. Method of measurement: Questionnaire -Complete a checklist to evaluate the symptoms of candidal vaginitis and then compare thefrequency of symptoms of candidal vaginitis within and between the two treatment groups.;Discharge. Timepoint: Start of study - 7 days after the start of the study. Method of measurement: Questionnaire.;Inflammation. Timepoint: Start of study - 7 days after the start of the study. Method of measurement: Questionnaire. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactSepideh Kermani
Islamic Azad University
Outcome results
None listed