Candida VulvoVaginitis. Candidiasis of vulva and vagina (N77.1*)
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Women were married and aged between 18-49 years old Not being pregnancy Not being lactation Not Having Allergy to Honey or Nigella Sativa or Clotrimazole Not being period Not using vaginal cream and vaginal doush and for last 48 hours before the study Not Having of history of diabetes and deficiency of immune system Not Having recurrent Candida vaginitis (4 or more Candida vaginitis in a year) Not Having of history of curettage, Hysterosalpingography and uterine surgery in the last two weeks No history of receiving blood or chemotherapy in a recent month Having of signs and symptoms of Candida vaginitis, positive direct smear and culther of vaginal discharge
Exclusion criteria
Exclusion criteria: Not Agreeing to Participate in the Study The use of antibiotics to treat non-vaginitis systemic infections during treatment Participation at another trial Pregnancy in the study time table
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Symptoms and signs of Candida Vulvovaginitis. Timepoint: Before intervention, 6-10 day after treatment. Method of measurement: Questionnaire,Microscopic evaluation,Secretion culture,Measurements Of Ph. | — |
Secondary
| Measure | Time frame |
|---|---|
| Improve Of Candida Vulvovaginitis. Timepoint: 6-10 Day After Treatment. Method of measurement: Questionnaire, culther. | — |
Countries
Iran (Islamic Republic of)
Contacts
Tehran University of Medical Sciences