Candidiasis vulvovaginitis. Vaginitis, vulvitis and vulvovaginitis in diseases classified elsewhere
Conditions
Interventions
Intervention 1: Intervention group: consist of 30 people who each receive a 2 gram vaginal suppository containing 0.1 cc of cuminum cyminum essential oil along with clotrimazole vaginal suppository da
Sponsors
Islamic Azad University
Eligibility
Sex/Gender
Female
Age
18 Years to 50 Years
Inclusion criteria
Inclusion criteria: Women aged 18 - 50 years old Being married Signature of consent Diagnosis of candidiasis infection lack of sensitivity to cuminum cyminum or clotrimazole
Exclusion criteria
Exclusion criteria: Pregnancy lactation menopause Underlying diseases Menstruation during the study Forget one dose or more of medication Allergy to clotrimazole or cuminum cyminum suppository The patient's unwillingness to continue treatment Abnormal uterine bleeding
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Itching. Timepoint: Beginning of the study - 7 days after the start of the study. Method of measurement: Questionnaire - completing a checklist to evaluate the symptoms of candidal vaginitis and then compare the frequency of symptoms of candidial vaginitis within and between the two treatment groups.;Discharge. Timepoint: Beginning of the study - 7 days after the start of the study. Method of measurement: Questionnaire.;Inflammation. Timepoint: Beginning of the study - 7 days after the start of the study. Method of measurement: Questionnaire. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactFatemehSadat Abtahi
Islamic Azad University
Outcome results
None listed