Cervicit. Inflammatory disease of cervix uteri
Conditions
Interventions
Intervention group: Patients treated with rose oil for two weeks will be given 3 ml of drug content every night..
Sponsors
Yazd University of Medical Sciences
Eligibility
Sex/Gender
Female
Age
17 Years to 55 Years
Inclusion criteria
Inclusion criteria: Women 17-55 years with a diagnosis of cervicit based on the opinion of a gynecologist Consent to participate in the study
Exclusion criteria
Exclusion criteria: Non-pregnancy and lactation No history of cervical polyps and pelvic surgery No simultaneous use of herbal or other chemicals
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Mean of Wound size. Timepoint: Before the intervention, after completion of the intervention. Method of measurement: Clinical examination.;Mean of Wound depth. Timepoint: Before the intervention, after completion of the intervention. Method of measurement: Clinical examination. | — |
Secondary
| Measure | Time frame |
|---|---|
| The amount of discharge. Timepoint: Before intervention, after intervention. Method of measurement: Clinical examination and patient based on VAS criteria.;Tenderness. Timepoint: Before intervention, after intervention. Method of measurement: Clinical examination.;Irritation. Timepoint: Before intervention, after intervention. Method of measurement: VAS criterion.;Itching. Timepoint: Before intervention, after intervention. Method of measurement: VAS criterion.;Pain after intercourse. Timepoint: Before intervention, after intervention. Method of measurement: Yes - no.;Post intercourse bleeding. Timepoint: Before intervention, after intervention. Method of measurement: Yes - no. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactZahra Dosthosseini
Yazd University of Medical Sciences
Outcome results
None listed