DeVEnIR: Defining Vulvovaginal Candidiasis - Elements of Infection and Remedy

Status: Recruiting
Location: See all (3) locations...
Intervention Type: Other
Study Type: Observational
SUMMARY

Female-specific health conditions are underrepresented in research. The taboo felt by women to talk about intimate wellbeing is fed by this gender gap in scientific knowledge. This project aims to meet these needs by studying one of the most prevalent female-specific infections, vulvovaginal candidiasis (VVC), and paving the way towards its efficient diagnosis and treatment. About 70% of women worldwide suffer from vaginal candidiasis at least once in their life. An episode of this fungal infection is accompanied by a burning sensation, pain, and reduced mental well-being. Some women (about 5%) encounter such infections at least four times a year, referring to recurrent(R) VVC. The design of efficient diagnostic and therapeutic strategies for (R)VVC is hindered by a knowledge gap surrounding vaginal health. To meet the absolute need for more information, this project will characterize the role of the microbiome, metabolome, immune system, and pathogen characteristics in (R)VVC. To this end, a large sampling platform of women with/without VVC will be established in this project. The researchers will identify the most important and clinically relevant microorganisms, metabolites, and immune factors in VVC pathogenesis. VVC models will be developed and optimized, which will be used to validate the causality of the correlations identified in the cohort. Identified correlations will be proposed as biomarkers, and microbes, metabolites, and combinations, which effectively lower the pathogenicity of Candida species, will be further investigated for therapeutic potential. State-of-the-art tools and know-how of the researchers will allow the unraveling of the involved molecular pathways and elucidate how these can be exploited to optimize therapeutic efficacy. Finally, the knowledge gathered in this project will be used to improve the literacy of women on VVC using platforms established by the researchers as well as novel tools to be developed in this project.

Eligibility
Participation Requirements
Sex: Female
Minimum Age: 18
Maximum Age: 50
Healthy Volunteers: t
View:

• Female

• Age: 18-50

• Premenopausal

Locations
Other Locations
Belgium
University of Antwerp
RECRUITING
Antwerp
University of Antwerp
RECRUITING
Antwerp
Femicare vzw
RECRUITING
Tienen
Contact Information
Primary
Gilbert Donders, Professor
gilbert.donders@femicare.net
+3216 80 81 02
Backup
Veronique Verhoeven, Professor
veronique.verhoeven@uantwerpen.be
+3232652518
Time Frame
Start Date: 2024-05-22
Estimated Completion Date: 2025-05
Participants
Target number of participants: 500
Treatments
Healthy women
Healthy volunteers that do not have vaginal complaints or symptoms, and did not have any in the past 12 months.
Women with an acute episode of vulvovaginal candidiasis
Women that have sporadic/acute vulvovaginal Candida infection. It's the first time or the first time in a longer period (1-2 years) that these women have an infection.
Women that suffer from recurrent episodes of vulvovaginal candidiasis
These women encounter such infections at least 3 times a year. These women are targeted both during an infection and in between infections.
Related Therapeutic Areas
Sponsors
Leads: University Hospital, Antwerp
Collaborators: Universiteit Antwerpen, Leibniz Institute for Natural Product Research and Infection Biology Hans Knöll Institute, Research Foundation Flanders, KU Leuven

This content was sourced from clinicaltrials.gov