exocervisitis. Vaginitis, vulvitis and vulvovaginitis in diseases classified elsewhere
Conditions
Interventions
Intervention 1: Intervention group: if this patient had the inclusion criteria, after submitting a description and obtaining informed consent, received a vaginal gel containing 7.5% of propolis extrac
Sponsors
Esfahan University of Medical Sciences
Eligibility
Sex/Gender
Female
Age
18 Years to 45 Years
Inclusion criteria
Inclusion criteria: Iranian race. 18-45 years old. Be sexually active( married). Had one sexual partner. Not pregnant or lactating. Not during menstruation period. Positive wet smear in both groups. A gynecologist confirmation of diagnosis. Not having a history of drug allergy. Not having a history of using antibiotics or vaginal drugs for ectocervicitis treatment in last 1 months ago. Not having a history of using hormonal and immunosuppressive drugs. Not having a history of some diseases such as: chronic diabetes melitus, anemia, renal diseases, liver diseases, cardiovascular diseases and etc... Not having a history of pelvic surgery.
Exclusion criteria
Exclusion criteria: Not interested in participating in the study. Not referred for follow up visits. Irregular used of drugs (two consecutive nights or three not-consecutive nights). Used of other antibiotics. Used of other palliative treatment. Having sexual function without used of condom.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Healing of trichomonas ectocervisiti. Timepoint: Pre intervention,1 and 2 weeks after intervention. Method of measurement: Self-made questionnaire. | — |
Secondary
| Measure | Time frame |
|---|---|
| Healing of trichomonas ectocervisitis. Timepoint: Preintervention,1 and 2 weeks after intervention. Method of measurement: Self-made questionnaire. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactSeyedeh Shadi Taghavian
Esfahan University of Medical Sciences
Outcome results
None listed