Cervicitis. Inflammatory disease of cervix uteri
Conditions
Interventions
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Treatment - Drugs
Use an applicator of traditional medicine products discurainia sophia honey for two weeks
Sponsors
School of Traditional Medicine and Materia Medica Research Center Shahid Beheshti
Eligibility
Sex/Gender
Female
Age
17 Years to 55 Years
Inclusion criteria
Inclusion criteria: Inclusion criteria: women aged 17-55 with cervicitis; diagnosed by a gynecologist, who did not respond to antibiotic treatment or have relapsed during the past 6 months and are willing to participate in the study. Exclusion criteria: pregnancy; lactation; addiction; a history of pelvic surgery; cervical polyps; any other chronic disorder associated with cervix; previous Pap smear with abnormal cells; or concomitant use of herbal or chemical drugs for his illness. Exclusion criteria during the study that there is a Pap test result of abnormal cells; patients who are experiencing side effects; patients need to have surgery or other interventions; patients with a personal question have decided to withdraw from the study.
Exclusion criteria
Exclusion criteria:
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Cervical ulcer size. Timepoint: Before the intervention, after intervention. Method of measurement: Physical examination.;The depth of the ulcer. Timepoint: Before the intervention, after intervention. Method of measurement: Physical examination. | — |
Secondary
| Measure | Time frame |
|---|---|
| Endocervical discharge culture. Timepoint: Before the intervention, after intervention. Method of measurement: Culture results based on laboratory results.;Vaginal discharge culture. Timepoint: Before the intervention, after intervention. Method of measurement: Culture results based on laboratory results.;Adenexal tenderness. Timepoint: Before the intervention, after intervention. Method of measurement: Physical examination.;Discharge. Timepoint: Before the intervention, after intervention. Method of measurement: Physical examination and patient based on VAS.;Burning. Timepoint: Before the intervention, after intervention. Method of measurement: VAS (visual analoge scale).;Itching. Timepoint: Before the intervention, after intervention. Method of measurement: VAS.;Pain during intercourse. Timepoint: Before the intervention, after intervention. Method of measurement: Pos/Neg.;Post coital bleeding. Timepoint: Before the intervention, after intervention. Method of measurement: Pos/Neg. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactNabimeybodi Razieh
Traditional Medicine and Materia Medica Research Center, Department of Traditional Medicine, School
Outcome results
None listed