Effect of Vaginal Product of Descurainia sophia- Honey derived from Iranian Traditional Medicine on Clinical and Laboratory in Patients with Cervicitis
Phase 2
- Conditions
- Cervicitis.Inflammatory disease of cervix uteri
- Registration Number
- IRCT2015110824951N1
- Lead Sponsor
- School of Traditional Medicine and Materia Medica Research Center Shahid Beheshti
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- Female
- Target Recruitment
- 80
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
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method 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 Outcome Measures
Name Time Method 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.