Women's Health in Women's Hands
Toronto, Ontario, M5B1J3, Canada
NCT Number: NCT03837015
This study will enrol African, Caribbean and Black (ACB) women who are known to have a more diverse vaginal microbiome, higher rates of bacterial vaginosis with lower numbers of protective lactobacilli, and are at increased risk for HIV. The investigators will evaluate the safety, feasibility, effect on the vaginal bacterial microbiome and changes in local immune and inflammatory responses with the administration of vaginal estrogen alone, vaginal estrogen in combination with oral or vaginally administered probiotics, or vaginal probiotics alone.
Looking for future studies?
Notify Me18 year–49 year
Female
Interventional
Phase 1
Toronto, Ontario, M5B1J3, Canada
Women are at increased risk of HIV acquisition compared with men. A number of biological factors are associated with increased risk, many of which likely enhance risk by increasing inflammation in the female genital tract. Susceptibility to infections and immune responses in the female genital tract are regulated by hormones: progesterone increases inflammation and HIV susceptibility and estrogen decreases inflammation and enhances colonization with Lactobacilli.
A Lactobacillus dominant vaginal microbiome is associated with increased protection against HIV, while a polymicrobial vaginal flora, as seen in bacterial vaginosis, is associated with increased risk. About 40% of ACB women have a polymicrobial flora.
The goal of this study is to establish a Lactobacillus dominant vaginal microbiome in ACB women, that will be associated with decreased inflammation and decreased susceptibility to HIV, by administering a low level of intravaginal estrogen to increase colonization with Lactobacilli together with a Lactobacillus-containing probiotic.
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Estradiol vaginal ring, containing 2mg estradiol designed for slow release over 30 days
Other names: 17 beta-estradiol
Probiotic supplement containing 2.5 billion CFU of Lactobacilli reuteri RC-14 and Lactobacilli rhamnosus GR-1, administered vaginally or orally
Time frame: 12 months
Number of eligible participants approached who do not consent to be enrolled
Time frame: 12 months
Number of participants who complete the study as proportion of total number of participants enrolled
Time frame: 2 months
The incidence of adverse events, including serious adverse events, their severity and their relationship to study intervention assessed by reviewing case report forms and participant diaries.
Time frame: 30 days
Adherence will be measured by calculating the total probiotic used/total dispensed and for Estring by total days used/total time period
Time frame: 30 days
Aliquots of cervico-vaginal lavage (CVL) fluids will undergo microbiome analysis using a modified Illumina sequencing method for bacterial community profiling of 16S rRNA to measure changes from baseline at follow-up sampling.
Time frame: 30 days
Changes from baseline in levels of cytokine/chemokines will be measured in CVL by a 22-plex multiplex assay at 2 and 4 weeks
Time frame: 30 days
Changes from baseline in level of HIV susceptible CD4+ T cells will be quantified using a lab developed HIV pseudovirus assay at 2 and 4 weeks.
McMaster University
Other
Improving Vaginal Health to Decrease Biological Risk of HIV-1 Infection in Canadian African, Caribbean and Black (ACB) Women: Estrogen and Probiotic Treatment for Vaginal Health
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
Published trials that share one or more normalized conditions with this study.
NCT05601128
Blood-Borne Infections, Communicable Diseases
Pittsburgh, Pennsylvania, United States
View Trial DetailsNCT05471076
HIV-1-infection
Birmingham, Alabama, United States
View Trial DetailsNCT05405582
Communicable Diseases, Disease Attributes
Somkele, KwaZulu-Natal, South Africa
View Trial DetailsNCT04067869
Cytomegalovirus Infections, DNA Virus Infections
Bordeaux, France
View Trial Details