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Completed

NCT Number: NCT03837015

Estrogen, Probiotics and Vaginal Health to Prevent HIV Infection in ACB Women

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.

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Key information

Age range

18 year–49 year

Sex eligibility

Female

Study type

Interventional

Phase

Phase 1

Primary location

Women's Health in Women's Hands

Toronto, Ontario, M5B1J3, Canada

About this study

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.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • African, Caribbean, Black
  • Pre-menopausal women in good general health, as determined by the investigator
  • Uterus and cervix present
  • Negative pregnancy test
  • Currently practicing barrier or non-hormonal forms of contraception, and planning to continue, for the duration of the study (barrier contraceptive, abstinence)
  • Willing to undergo a pelvic exam by a female nurse/female doctor
  • Willing to abstain from vaginal intercourse for 48 hours prior to sampling, over the entire course of the study
  • Able to understand, comply and consent to protocol requirements and instructions
  • Able to attend scheduled study visits and complete required investigations

Exclusion criteria

  • Currently lactating
  • Pregnant: suspected, current or in the last 12 months
  • Irregular menstrual cycle (less than 6 periods in a year) not related to contraceptive use, pregnancy or breastfeeding
  • Post-menopausal
  • Hormonal Contraceptive use or other hormonal treatment in the past 3 months
  • Current Intra-Uterine Device (IUD) use
  • Positive test result for Gonorrhea and/or Chlamydia
  • Clinically obvious genital ulceration/lesions
  • Symptomatic vaginal yeast infection or clinically significant vaginal discharge
  • HIV-positive
  • Any clinically significant abnormality on screening safety blood tests, that in the opinion of the investigator would preclude enrolment.
  • Diagnosed blood clotting disorder
  • Any genital tract procedure (e.g. biopsy) within the past 6 months
  • Use of oral probiotic supplement, oral antibiotics or oral steroids within the past 30 days
  • Current use of any vaginal products (except tampons) such as spermicides, microbicides, douching or drying products, antifungals, or steroids.
  • Known intolerance of Lactobacillus-containing probiotic supplements
  • Undiagnosed abnormal genital bleeding
  • Known, suspected, or history of breast cancer
  • Known or suspected estrogen-dependent malignant neoplasia (e.g. endometrial cancer)
  • Currently taking immunosuppressive drugs
  • Known or suspected hypersensitivity to any component of the Estring or RepHresh Pro-B products
  • Diagnosis of endometrial hyperplasia
  • Known liver dysfunction or disease; as long as liver function tests have failed to return to normal
  • Active or past history of arterial thromboembolic disease (e.g. stroke, myocardial infarction, coronary heart disease)
  • Partial or complete loss of vision due to ophthalmic vascular disease
  • Porphyria
  • Concomitant medication which in the opinion of the investigator may be associated with a significant drug interaction with the estrogen in Estring.
  • The conditions below are grounds for exclusion based on the opinion of the investigator:
  • Risk factors for estrogen dependent tumours, e.g. first degree heredity for breast cancer
  • Diabetes mellitus with or without vascular involvement
  • Migraine or (severe) headache
  • Epilepsy
  • A history of, or risk factors for, thromboembolic disorders
  • Systemic lupus erythematosus
  • Otosclerosis
  • Cholelithiasis
  • Leiomyoma (uterine fibroids)
  • Endometriosis
  • A history of endometrial hyperplasia
  • Hypertension
  • Asthma
  • Diagnosed anemia

Treatment and study plan

Estring Vaginal Ring

Drug

Estradiol vaginal ring, containing 2mg estradiol designed for slow release over 30 days

Other names: 17 beta-estradiol

RepHresh Pro-B

Other

Probiotic supplement containing 2.5 billion CFU of Lactobacilli reuteri RC-14 and Lactobacilli rhamnosus GR-1, administered vaginally or orally

Primary outcomes

  1. Refusal rate

    Time frame: 12 months

    Number of eligible participants approached who do not consent to be enrolled

  2. Participant retention rate

    Time frame: 12 months

    Number of participants who complete the study as proportion of total number of participants enrolled

  3. Incidence of treatment emergent adverse events

    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.

  4. Rate of adherence

    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

Secondary outcomes

  1. Changes in proportion of Lactobacillus species in the vaginal microbiota

    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.

  2. Change in innate inflammatory cytokine/chemokine levels

    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

  3. Changes in number of HIV target cells in the genital tract

    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.

Sponsors and collaborators

Lead sponsor

McMaster University

Other

Collaborators

  • CIHR Canadian HIV Trials Network

Registry information

Official study title

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

Important dates

Study start
2019
Primary completion
2021
Study completion
2021
First posted
Feb 11, 2019
Registry last updated
Dec 17, 2021

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.

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