''The effect of Rose oil in women with cervicitis''
Phase 2
Recruiting
- Conditions
- Cervicit.Inflammatory disease of cervix uteri
- Registration Number
- IRCT20190810044500N1
- Lead Sponsor
- Yazd University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Female
- Target Recruitment
- 52
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
Non-pregnancy and lactation
No history of cervical polyps and pelvic surgery
No simultaneous use of herbal or other chemicals
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method 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 Outcome Measures
Name Time Method 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.