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Epidemiological Study in Subjects With Vulvovaginal Candidiases

Estudio epidemiológico de la evolución clínica y microbiológica en Pacientes Tratadas Por un Episodio Agudo de Candidiasis Vulvovaginal

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03064789
Enrollment
43
Registered
2017-02-27
Start date
2016-12-29
Completion date
2019-06-30
Last updated
2021-02-11

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Vulvovaginal Candidiases

Keywords

Candidiases, Vaginal Infections

Brief summary

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

Interventions

None listed

Sponsors

Dr. Santiago Palacios
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 50 Years
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frameDescription
Estimate cure rate in women with severe vuvovaginal candidiases infectionAt 3 monthsWomen must require antimicotic treatment plus vaginal probiotic following the habitual therapeutic standards

Secondary

MeasureTime frameDescription
Estimate recurrencesAt 6 monthsIt will be consider recurrences an asymptomatic period for 7-10 days and a negative culture
Evaluate the link between symptomatology and negative cultureAt 3 months
Evaluate the effectiveness of probiotic treatment by physicianAt 3 monthsA gynecological exploration will be performed
Evaluate the effectiveness of probiotic treatment by patient. A satisfaction questionnaire will be performedAt 3 monthsThe subject will be asked how long the symptoms lasted and the gravity of them

Countries

Spain

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026