Randomize comparison of vaginal suppository containing cuminum cyminum essential oil with vaginal clotrimazole versus placebo vaginal suppository for vulvovaginal candidiasis treatment

Phase 1

Recruiting

• Conditions: Candidiasis vulvovaginitis.; Vaginitis, vulvitis and vulvovaginitis in diseases classified elsewhere; N77.1

• Registration Number: IRCT20150706023084N11
• Lead Sponsor: Islamic Azad University

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 1 November 2021

Recruitment & Eligibility

• Status: Recruiting
• Sex: Female
• Target Recruitment: 60

Inclusion Criteria

Women aged 18 - 50 years old
Being married
Signature of consent
Diagnosis of candidiasis infection
lack of sensitivity to cuminum cyminum or clotrimazole

Exclusion Criteria

Pregnancy
lactation
menopause
Underlying diseases
Menstruation during the study
Forget one dose or more of medication
Allergy to clotrimazole or cuminum cyminum suppository
The patient's unwillingness to continue treatment
Abnormal uterine bleeding

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Itching. Timepoint: Beginning of the study - 7 days after the start of the study. Method of measurement: Questionnaire - completing a checklist to evaluate the symptoms of candidal vaginitis and then compare the frequency of symptoms of candidial vaginitis within and between the two treatment groups.;Discharge. Timepoint: Beginning of the study - 7 days after the start of the study. Method of measurement: Questionnaire.;Inflammation. Timepoint: Beginning of the study - 7 days after the start of the study. Method of measurement: Questionnaire.