Phase
Condition
N/ATreatment
N/AClinical Study ID
Ages > 10 All Genders Accepts Healthy Volunteers
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria of Central Participants:
Adults aged 18 and over at the time of enrollment;
Sex: Female;
Pre-menopausal;
Self-reported good health (including the absence of general infection);
Absence of reproductive disorders (e.g. endometriosis, polycystic ovary syndrome), vaginal infections and symptoms diagnosed by a medical professional;
Absence of gastrointestinal disorders, infections and symptoms diagnosed by a medical professional;
Sufficient knowledge of the Dutch language;
Consent form signed;
Participating alongside her mother and at least one additional co-participant in the study.
Exclusion Criteria of Central Participants:
Current pregnancy or planned pregnancy at the beginning and during of the study;
Breastfeeding at the start and during the study;
Current diagnosis of cancer and/or immunosuppressive therapy in the 6 months before the study;
Clinically significant abnormalities of the reproductive organs or any other medical condition at the discretion of the principal investigator;
Use of oral/vaginal antibiotics/antifungals in the 2 months before and during the study;
Use of oral/vaginal pre- and/or probiotics in the 2 weeks before the study and during the study;
Vaginal showering during the study;
Participation in an intervention study.
Inclusion Criteria of Co-participants:
Closely related to or interacting with the central participant of the network at least during the last six months or more before the study, e.g. her mother, aunts, female cousins, sisters, daughters, housemates, partners or close friends;
Aged 18 or over at the time of enrollment; OR 10 or over if the co-participant's mother is also participating in the study;
Sex: Female; OR male aged 18 and over who is the partner or one of the partners (in case of polygamous relationships) of the central participant;
Self-reported good health (including the absence of general infection);
Sufficient knowledge of the Dutch language;
Consent form signed.
Exclusion Criteria of Co-participants:
Use of oral/vaginal antibiotics/antifungals in the 2 months before the study;
Parallel participation in an intervention study;
Vaginal showering during the study;
Clinically significant abnormalities of the reproductive organs or any other medical condition that, in the opinion of the principal investigator, warrants exclusion from the study.
Study Design
Connect with a study center
University of Antwerp
Antwerp, 2020
BelgiumActive - Recruiting
Not the study for you?
Let us help you find the best match. Sign up as a volunteer and receive email notifications when clinical trials are posted in the medical category of interest to you.