Evaluation of the effectiveness of black seed oil in the treatment of vulvovaginal mucositis

Phase 3

Recruiting

Conditions: Inflammation of the vulvovaginal mucosa.
Vaginitis, vulvitis and vulvovaginitis in diseases classified elsewhere
N77.1

Registration Number: IRCT20200720048145N2

Lead Sponsor: Alborz University of Medical Sciences

Brief Summary: Not available

Detailed Description: Not available

Recruitment & Eligibility

Status: Recruiting

Sex: Female

Target Recruitment: 100

Inclusion Criteria

Age 15-60 years
Do not using immunosuppressive drugs, antibiotics and topical creams and ointments during the last week
Do not be pregnant or breastfeeding
Normal Pap smear test

Exclusion Criteria

Allergy to the drug prescribed to the patient
Failure to follow treatment regularly and as directed
Mandatory administration of antibiotics by another physician outside the scope of the present study
Having sex with multiple partners during treatment

Study & Design

Study Type: interventional

Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Inflammation of the vagina. Timepoint: In two stages before the intervention and after the intervention. Method of measurement: Examination of the vagina.

Secondary Outcome Measures

Name	Time	Method
Vaginal discharge. Timepoint: Before and 7 days after the start of the intervention. Method of measurement: Questionnaire.;Vaginal itching. Timepoint: Before and 7 days after the start of the intervention. Method of measurement: Questionnaire.;Bad smell of vaginal discharge. Timepoint: Before and 7 days after the start of the intervention. Method of measurement: Questionnaire.;Vaginal burning. Timepoint: Before and 7 days after the start of the intervention. Method of measurement: Questionnaire.;Painful intercourse. Timepoint: Before and 7 days after the start of the intervention. Method of measurement: Questionnaire.;Urinary incontinence. Timepoint: Before and 7 days after the start of the intervention. Method of measurement: ????????.