In vivo evaluation of vaginal suppository containing corianderum sativum essential oil effect on the treatment of candidiasis infectio

Phase 1

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

• Registration Number: IRCT20150706023084N8
• Lead Sponsor: Islamic Azad University

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 22 February 2021

Recruitment & Eligibility

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

Inclusion Criteria

age 18-50
Diagnosis of candidiasis infection
Signature of consent

Exclusion Criteria

Pregnancy, lactation, menopause, underlying diseases
Sex during the study
Forget a dose or more of medication
Allergy to clotrimazole or coriander suppository
The patient's unwillingness to continue treatment

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Itching. Timepoint: Start of study - 7 days after the start of the study. Method of measurement: Questionnaire three-Complete a checklist to evaluate the symptoms of candidal vaginitis and then compare the frequency of symptoms of candidal 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 three.;Inflammation. Timepoint: Beginning of the study - 7 days after the start of the study. Method of measurement: Questionnaire three.