candida vaginitis.
Conditions
Interventions
Intervention 1: Intervention group: Nivasha spray containing 50 cc solution of silver nanoparticles with a concentration of 15 ppm for 10 consecutive days and once a day and 3 puffs each time is pres
Sponsors
Esfahan University of Medical Sciences
Eligibility
Sex/Gender
Female
Age
15 Years to 49 Years
Inclusion criteria
Inclusion criteria: Women of childbearing age 15-49 years Married women Consent to participate in the study Be literrat No pregnancy No breast feeding and menopause Having 2 symptoms of candida vaginitis (vaginal discharge, itching) Healthy women (without known immunosuppressive disease, hypertension, diabetes mellitus) Don’t use of herbal and chemical drugs for vaginitis during recent 2 weeks No other vaginal infections such as trichomoniasis Don’t use of any vaginal cream 48 hours before onset of study No participation in another study at the same time as the present study Do not use antibiotics and corticosteroids for the past two weeks No report of allergy to Nivasha spray (containing silver) (if used previously) and clotrimazole (if used previously) Getting Candida Vaginitis for the First Time
Exclusion criteria
Exclusion criteria: Mensturation at onset of study AUB Antibiotice use for systemic infections during study
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Vulvar itching. Timepoint: Every day for 10 days. Method of measurement: Vaginal exam - Self report.;Vulvar redness. Timepoint: Every day for 10 days. Method of measurement: Vaginal exam - Self report.;White cheese discharge. Timepoint: Every day for 10 days. Method of measurement: Vaginal exam - Self report. | — |
Secondary
| Measure | Time frame |
|---|---|
| Vulvar edema. Timepoint: Every day for 10 days. Method of measurement: Vaginal exam - self report. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactMaryam Kianpour
Esfahan University of Medical Sciences
Outcome results
None listed