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Effects of Flourish HEC and BioGenesis to Improve Conception

Primary Purpose

Infertility, Infertility Unexplained

Status
Terminated
Phase
Phase 1
Locations
United States
Study Type
Interventional
Intervention
Flourish HEC and BioGenesis
Sponsored by
Vaginal Biome Science
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional other trial for Infertility

Eligibility Criteria

18 Years - 40 Years (Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria:

Women part of a cisgender couple aged 18 to 40 who are attempting to become pregnant and are attending a fertility clinic.

Exclusion Criteria:

  1. Pregnant
  2. Lactating
  3. Severe male factor, hormonal imbalance (oligoovulatory/anovulatory cycles, cycles longer than 35 days), genetic abnormalities (chromosomal abnormality, common genetic mutation between partners), or severe uterine or tubal factor
  4. Any diagnosis that would require the participant to undergo in vitro fertilization to become pregnant
  5. Known allergies to any component of BioNourish®, Balance, BiopHresh®, or BioGenesis™
  6. Known active vaginal infection at enrollment

Sites / Locations

  • Dr. Aimee Eyvazzadeh

Arms of the Study

Arm 1

Arm 2

Arm Type

No Intervention

Experimental

Arm Label

Control arm

Flourish HEC + BioGenesis arm

Arm Description

Women follow routine care only, including prescribed medications and recommended techniques and supplements for attempting to become pregnant at home for up to three months.

In addition to routine care followed by women in control arm, women in this arm also use the Flourish HEC (Hydroxyethylcellulose) vaginal care system and BioGenesis fertility lubricant for up to three months.

Outcomes

Primary Outcome Measures

Conception at home
Percentage of women becoming pregnant at home within the 3 month study.
Change in vaginal microbiome
Vaginal microbiome composition tested by next-generation sequencing
Change in vaginal pH
Vaginal pH tested by vaginal fluid applied to pH test strip

Secondary Outcome Measures

Conception within one year
Percentage of women becoming pregnant by any method within the 3 month study or within one year after ending the study.
Rate of live birth
Percentage of women giving live birth within one year after ending the study; or if pregnant at one year, following to the end of her pregnancy.
Gestational age at delivery
Average gestational age of babies born within one year after ending the study; or if mothers are pregnant at one year, following to the end of her pregnancy.
Birthweight at delivery
Average weight of babies born within one year after ending the study; or if mothers are pregnant at one year, following to the end of her pregnancy.
Rates of pregnancy complications
Percentage of women experiencing complications (including preeclampsia, miscarriage/fetal loss/stillbirth, preterm/premature rupture of membranes, chorioamnionitis or endometritis, gestational diabetes, and any other adverse outcome) within one year after ending the study; or if mothers are pregnant at one year, following to the end of her pregnancy.

Full Information

First Posted
May 18, 2022
Last Updated
July 17, 2023
Sponsor
Vaginal Biome Science
Collaborators
Dr. Aimee Eyvazzadeh, Inc.
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1. Study Identification

Unique Protocol Identification Number
NCT05390606
Brief Title
Effects of Flourish HEC and BioGenesis to Improve Conception
Official Title
Pilot Study: Effects of Flourish HEC Vaginal Care System and BioGenesis Fertility Lubricant on Conception
Study Type
Interventional

2. Study Status

Record Verification Date
July 2023
Overall Recruitment Status
Terminated
Why Stopped
Lack of enrollment
Study Start Date
June 15, 2022 (Actual)
Primary Completion Date
March 20, 2023 (Actual)
Study Completion Date
March 20, 2023 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Vaginal Biome Science
Collaborators
Dr. Aimee Eyvazzadeh, Inc.

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
Yes
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
This study intends to address whether improving the vaginal microbiome can help couples increase chances of conceiving.
Detailed Description
Disrupted vaginal microbiomes are associated with a number of poor reproductive outcomes, including infertility, miscarriage, premature rupture of membranes, preterm labor and delivery, delivery of a low birthweight baby, and maternal infections (chorioamnionitis, endometritis). A healthy vaginal microbiome is typically thought to be one that is dominated by one of several Lactobacillus species, such as L. crispatus, L. gasseri, or L. jensenii. Several studies have shown that non-lactobacilli-dominant biomes are associated with poor in vitro fertilization or intrauterine insemination outcomes. Fewer studies have examined fertility in the home setting, and none to date has asked whether improving the vaginal microbiome (VMB) could increase fertility. This study addresses both. By assessing the VMB before and after using a vaginal care system which supports a healthy VMB, we will be able to examine whether there are associations between VMB composition and infertility, and whether shifting the VMB toward a lactobacillus-dominant state is able to improve chances of conception. In this study, women will either follow routine care (control) or routine care plus the vaginal care system and fertility lubricant (intervention) for 3 months or until becoming pregnant, whichever comes first. In addition to tracking conception rates during those 3 months, we will follow women for an additional year following completion of the 3-month timeframe. If any woman is pregnant at the one-year mark, her pregnancy will be followed until delivery (or early termination) to track delivery outcomes and adverse events.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Infertility, Infertility Unexplained

7. Study Design

Primary Purpose
Other
Study Phase
Phase 1
Interventional Study Model
Parallel Assignment
Model Description
A longitudinal open label randomized controlled trial.
Masking
None (Open Label)
Allocation
Randomized
Enrollment
1 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Control arm
Arm Type
No Intervention
Arm Description
Women follow routine care only, including prescribed medications and recommended techniques and supplements for attempting to become pregnant at home for up to three months.
Arm Title
Flourish HEC + BioGenesis arm
Arm Type
Experimental
Arm Description
In addition to routine care followed by women in control arm, women in this arm also use the Flourish HEC (Hydroxyethylcellulose) vaginal care system and BioGenesis fertility lubricant for up to three months.
Intervention Type
Combination Product
Intervention Name(s)
Flourish HEC and BioGenesis
Intervention Description
Flourish HEC is a 3-component system, including: 1) Balance feminine wash, used daily; 2) BioNourish vaginal moisturizer, used daily before bed except if having intercourse; 3) BiopHresh homeopathic vaginal suppository with probiotics, used once every 3 days before bed except if having intercourse. BioNourish is a class II medical device with FDA 510k clearance, on the market for 2 years. BioGenesis is also a class II medical device with FDA 510k clearance, and is designated as a fertility lubricant, safe for sperm and embryos.
Primary Outcome Measure Information:
Title
Conception at home
Description
Percentage of women becoming pregnant at home within the 3 month study.
Time Frame
3 months
Title
Change in vaginal microbiome
Description
Vaginal microbiome composition tested by next-generation sequencing
Time Frame
Baseline to end of active study period, which is either at 3 months or upon confirmation of pregnancy, whichever occurs first.
Title
Change in vaginal pH
Description
Vaginal pH tested by vaginal fluid applied to pH test strip
Time Frame
Baseline to end of active study period, which is either at 3 months or upon confirmation of pregnancy, whichever occurs first.
Secondary Outcome Measure Information:
Title
Conception within one year
Description
Percentage of women becoming pregnant by any method within the 3 month study or within one year after ending the study.
Time Frame
15 months
Title
Rate of live birth
Description
Percentage of women giving live birth within one year after ending the study; or if pregnant at one year, following to the end of her pregnancy.
Time Frame
24 months or fewer
Title
Gestational age at delivery
Description
Average gestational age of babies born within one year after ending the study; or if mothers are pregnant at one year, following to the end of her pregnancy.
Time Frame
24 months or fewer
Title
Birthweight at delivery
Description
Average weight of babies born within one year after ending the study; or if mothers are pregnant at one year, following to the end of her pregnancy.
Time Frame
24 months or fewer
Title
Rates of pregnancy complications
Description
Percentage of women experiencing complications (including preeclampsia, miscarriage/fetal loss/stillbirth, preterm/premature rupture of membranes, chorioamnionitis or endometritis, gestational diabetes, and any other adverse outcome) within one year after ending the study; or if mothers are pregnant at one year, following to the end of her pregnancy.
Time Frame
24 months or fewer

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
40 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Women part of a cisgender couple aged 18 to 40 who are attempting to become pregnant and are attending a fertility clinic. Exclusion Criteria: Pregnant Lactating Severe male factor, hormonal imbalance (oligoovulatory/anovulatory cycles, cycles longer than 35 days), genetic abnormalities (chromosomal abnormality, common genetic mutation between partners), or severe uterine or tubal factor Any diagnosis that would require the participant to undergo in vitro fertilization to become pregnant Known allergies to any component of BioNourish®, Balance, BiopHresh®, or BioGenesis™ Known active vaginal infection at enrollment
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Aimee Eyvazzadeh, MD, MS, MBA
Organizational Affiliation
Dr. Aimee Eyvazzadeh, Inc.
Official's Role
Principal Investigator
Facility Information:
Facility Name
Dr. Aimee Eyvazzadeh
City
San Ramon
State/Province
California
ZIP/Postal Code
94583
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No

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Effects of Flourish HEC and BioGenesis to Improve Conception

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