Clinical Trials Directory

Trials / Terminated

TerminatedNCT00915629

Prevention of Recurrent Vulvovaginal Candidiasis With Lactibiane Candisis 5M®

Status
Terminated
Phase
N/A
Study type
Interventional
Enrollment
134 (estimated)
Sponsor
PiLeJe · Industry
Sex
Female
Age
18 Years – 65 Years
Healthy volunteers
Not accepted

Summary

Vulvovaginal candidiasis (VVC) is a common infection among women that is associated with considerable morbidity and health-care cost. 75% of women will suffer of Candida infection for at least one time in their life. 20% of women who suffer from VVC will have ≥ 4 episodes of VVC during the one year prior to the survey. 80% of these VVC are caused by Candida albicans. Current treatments, based on imidazoles, face many failures or recurrences. The type of probiotic Lactobacillus may participate in the prevention of recurrent vulvo-vaginitis in reducing the proliferation of intestinal Candida albicans, its adherence to the vaginal walls, the potentiation of its propagation. The primary objective of this study was to investigate if our supplementary treatment could improve the initial cure rate after vaginal econazole therapy.

Conditions

Interventions

TypeNameDescription
DIETARY_SUPPLEMENTLactibiane candisis 5M2 gelules per day for 2 months then 1 gelule per day for 4 months

Timeline

Start date
2009-06-01
Primary completion
2010-01-01
Completion
2010-07-01
First posted
2009-06-08
Last updated
2021-04-20

Locations

1 site across 1 country: France

Source: ClinicalTrials.gov record NCT00915629. Inclusion in this directory is not an endorsement.