Evaluation of the effectiveness of oral lactobacillus acidophillus on treatment of women's yeast infections

Phase 2

• Conditions: Candidal vulvovaginitis.; Candidiasis of vulva and vagina; B37.3+

• Registration Number: IRCT138901303756N1
• Lead Sponsor: Ahvaz University Of Medical Scienses

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 22 February 2018

Recruitment & Eligibility

• Status: Complete
• Sex: Female
• Target Recruitment: 86

Inclusion Criteria

married ladies with sign and symptoms of vulvovaginal candidiasis
Exclusion criteria:
pregnancy; breast feeding; side effects of the drug and lack of patient's cooperation in the study

Exclusion Criteria

Not provided

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Compelet remission. Timepoint: 7days and 30 days after treatment. Method of measurement: Evauation of clinical symptom's remission with questionnaire.;Relapse of the symptoms. Timepoint: 30 days after treatment. Method of measurement: Evaluation of relapsing symptoms after primary remission with questionnaire.