Clinical trial on comparing the effect of vaginal Shallomine containing the pure fraction of shallot extract and clotrimazole in treatment of candidal vaginitis

Phase 2

• Conditions: Condition 1: Candidiasis. Condition 2: Candidiasis of vulva and vagin.; Candidiasis; Candidiasis of vulva and vagina; B37.3

• Registration Number: IRCT20190728044356N1
• Lead Sponsor: Ahvaz University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 5 January 2021

Recruitment & Eligibility

• Status: Complete
• Sex: Female
• Target Recruitment: 30

Inclusion Criteria

aged between 18 and 50 years
Be married
Have 1 spouse
Have consent to participate in the study
Not allergic to herbal medicines
Not allergic to clotrimazole
Be literate

Exclusion Criteria

They have been taken antibiotics and corticosteroids for the past two weeks, according to the participant
Have any sores or lumps in the cervix based on observation with speculum
Present use of other herbal medicines
Have abnormal uterine bleeding

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Percentage of people with candidal vaginitis. Timepoint: Examination of Candida in the patient's vaginal discharge before the intervention and one week after taking the drug. Method of measurement: culture and Laboratory diagnosis of Candida.