Epidemiological Study in Subjects With Vulvovaginal Candidiases

Dr. Santiago Palacios43 enrolled

Overview

Epidemiological study about the clinical and microbiological progress in subjects under treatment for a severe vulvovaginal candidiases episody

Study Type

OBSERVATIONAL

Enrollment

Conditions

Vulvovaginal Candidiases

Eligibility

Sex: FEMALEMin age: 18 YearsMax age: 50 Years

Medical Language ↔ Plain English

Inclusion Criteria: * Sexually active women between 18 and 50 years of age at time of screening * With diagnosis and symptomatology of VVC Exclusion Criteria: * Pregnant women * Diabetes Mellitus * Women witihin three months after a delivery or misbirth * Women with vaginal or genital infection symptomatology other than candidiases that needs antibiotic treatment * Vaginal probiotics use within last three months * Undiagnosed abnormal genital hemorrhage

Locations (1)

Instituto Palacios

Madrid, Spain

Outcomes

Primary Outcomes

Estimate cure rate in women with severe vuvovaginal candidiases infection

Women must require antimicotic treatment plus vaginal probiotic following the habitual therapeutic standards

Time frame: At 3 months

Secondary Outcomes

Estimate recurrences

It will be consider recurrences an asymptomatic period for 7-10 days and a negative culture

Time frame: At 6 months

Estimate recurrences

It will be consider recurrences an asymptomatic period for 7-10 days and a negative culture

Time frame: At 12 months

Evaluate the link between symptomatology and negative culture

Time frame: At 3 months

Evaluate the effectiveness of probiotic treatment by physician

A gynecological exploration will be performed

Time frame: At 3 months

Evaluate the effectiveness of probiotic treatment by patient. A satisfaction questionnaire will be performed

The subject will be asked how long the symptoms lasted and the gravity of them

Time frame: At 3 months

Data from ClinicalTrials.gov

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