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Impact of Vaginal Microbiome on Vaginal Absorption of Exogenous Progesterone: a Pilot Study. (PROGEBIOMA)

Primary Purpose

Infertility, Female

Status
Completed
Phase
Not Applicable
Locations
Spain
Study Type
Interventional
Intervention
MICROBIOME GENETIC ANALYSIS
VAGINAL PH VALUE
SERUM PROGESTERONE LEVELS
SERUM OESTRADIOL LEVELS
Sponsored by
Instituto Valenciano de Infertilidad, IVI VALENCIA
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Infertility, Female focused on measuring LUTHEAL PHASE SUPPORT, MICROBIOME, INFERTILITY, ONGOING PREGNANCY RATE, LIFE BIRTH RATE, ARTIFICIAL REPRODUCTION TREATMENT, EMBRYO TRANSFER

Eligibility Criteria

18 Years - 50 Years (Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria:

  • The subject must provide written informed consent prior to any study related procedures
  • Women ≤50 years old
  • BMI ≤ 25 kg/m2
  • Adequate endometrial thickness (>6.5mm) and pattern (Triple A structure) in the proliferative phase

Exclusion Criteria:

  • Uterine Pathology, adnexal pathology
  • Systemic diseases -

Sites / Locations

  • Ivi Valencia

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

FROZEN EMBRYO TRANSFER

Arm Description

Women who undergo an artificial cycle for frozen embryo transfer and receive luteal phase support.

Outcomes

Primary Outcome Measures

Vaginal Microbiome
Result of the microbiome genetic analysis in vaginal samples (nucleic acid extraction and genetic analysis)

Secondary Outcome Measures

Live birth
Live birth rate
Ongoing Pregnancy Rate
Success value in pregnancy after ultrasound confirmation of heartbeat and 12 weeks of pregnancy
Clinical Pregnancy
Pregnancy confirmation by the observation of the presence of at least one gestational sac on ultrasound
Serum progesterone value
Serum progesterone levels
Vaginal PH
Measure of vaginal pH levels

Full Information

First Posted
December 15, 2021
Last Updated
October 23, 2023
Sponsor
Instituto Valenciano de Infertilidad, IVI VALENCIA
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1. Study Identification

Unique Protocol Identification Number
NCT05161338
Brief Title
Impact of Vaginal Microbiome on Vaginal Absorption of Exogenous Progesterone: a Pilot Study.
Acronym
PROGEBIOMA
Official Title
Impact of Vaginal Microbiome on Vaginal Absorption of Exogenous Progesterone: a Pilot Study.
Study Type
Interventional

2. Study Status

Record Verification Date
October 2023
Overall Recruitment Status
Completed
Study Start Date
February 15, 2022 (Actual)
Primary Completion Date
March 1, 2023 (Actual)
Study Completion Date
April 30, 2023 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Instituto Valenciano de Infertilidad, IVI VALENCIA

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Is already demonstrated that around 30% of patients undergoing an artificial cycle with vaginal progesterone do not reach a minimum threshold value of serum progesterone levels on the day of embryo transfer. Women with serum progesterone levels below this threshold have 20% lower ongoing pregnancy and live birth rates, decreasing their chances of success. However, the cause of this high heterogeneity in exogenous vaginal progesterone absorption among our patients remains unknown. It has been suggested that vaginal microbiome, and vaginal pH (due to its impact in microbiota growth), may explain the differences in vaginal progesterone absorption. The aim of the present pilot study is to assess if certain vaginal conditions, such as its microbiome status or its pH level, might affect vaginal progesterone absorption (measured by serum progesterone levels) and, in turn, the chances of success. In order to evaluate it, a prospective cohort unicentric study will be conducted in IVI RMA Valencia (Spain). Infertile patients undergoing an embryo transfer in the context of an artificial cycle when using vaginal progesterone will be recruited. Serum progesterone and estradiol levels, microbiome genetic analysis in vaginal samples and vaginal pH will be measured both on the embryo transfer-scheduling day and on the embryo transfer day.
Detailed Description
Currently, as part of routine clinical practice serum progesterone levels were meassured of women undergoing an ET in the context of an artificial cycle. These blood tests are usually performed around 2 hours before ET, thus results are available before their departure of the clinic. In the event of detecting low serum progesterone levels, an extra dose of exogenous subcutaneous progesterone is given for LPS. There is not knowing about the reason of this heterogeneity in progesterone absorption, and one plausible hypothesis is vaginal microbiome. In the event of proving a significant association between vaginal microbiome and serum progesterone levels on the day of ET, and in particular if these levels are below or above the delimited threshold, it would be possible to individualize LPS in several patients in a more direct manner. It is true that our current clinical practice, giving subcutaneous progesterone, is capable of equaling OPR of women with serum progesterone levels below 8.8 ng/ml on the ET day to those with values above this threshold applying the exact same approach to all patients. This study could be the next step towards an iLPS, to know the reason of the lower progesterone levels, and treat it directly, instead of moving to the need of a daily injection of progesterone which is costly and not patient friendly. Furthermore, vaginal microbiome may also have an impact in the subsequent OPR, even though serum progesterone levels were over 8.8 ng/ml. If this is the case, the analisys in advance the patient's vaginal microbiome will allow to treat the patient accordingly in order to increase the results of the ART treatment.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Infertility, Female
Keywords
LUTHEAL PHASE SUPPORT, MICROBIOME, INFERTILITY, ONGOING PREGNANCY RATE, LIFE BIRTH RATE, ARTIFICIAL REPRODUCTION TREATMENT, EMBRYO TRANSFER

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Model Description
Prospective cohort unicentric pilot study
Masking
None (Open Label)
Allocation
N/A
Enrollment
100 (Actual)

8. Arms, Groups, and Interventions

Arm Title
FROZEN EMBRYO TRANSFER
Arm Type
Experimental
Arm Description
Women who undergo an artificial cycle for frozen embryo transfer and receive luteal phase support.
Intervention Type
Diagnostic Test
Intervention Name(s)
MICROBIOME GENETIC ANALYSIS
Intervention Description
Vaginal samples will be taken. A floxed nylon swab will be rotated against the posterior vaginal wall, Nucleic acid extraction and genetic analisys will be performed
Intervention Type
Diagnostic Test
Intervention Name(s)
VAGINAL PH VALUE
Intervention Description
Intravaginal Ph value meassurement.
Intervention Type
Diagnostic Test
Intervention Name(s)
SERUM PROGESTERONE LEVELS
Intervention Description
Determination of serum P4 levels On the day of embryo transfer scheduling (prior to the onset of exogenous progesterone administration) and on the embryo transfer day-.
Intervention Type
Diagnostic Test
Intervention Name(s)
SERUM OESTRADIOL LEVELS
Intervention Description
Determination of serum E2 levels On the day of embryo transfer scheduling (prior to the onset of exogenous progesterone administration) and on the embryo transfer day.
Primary Outcome Measure Information:
Title
Vaginal Microbiome
Description
Result of the microbiome genetic analysis in vaginal samples (nucleic acid extraction and genetic analysis)
Time Frame
12 months
Secondary Outcome Measure Information:
Title
Live birth
Description
Live birth rate
Time Frame
12 months
Title
Ongoing Pregnancy Rate
Description
Success value in pregnancy after ultrasound confirmation of heartbeat and 12 weeks of pregnancy
Time Frame
12 months
Title
Clinical Pregnancy
Description
Pregnancy confirmation by the observation of the presence of at least one gestational sac on ultrasound
Time Frame
12 months
Title
Serum progesterone value
Description
Serum progesterone levels
Time Frame
12 months
Title
Vaginal PH
Description
Measure of vaginal pH levels
Time Frame
12 months

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
50 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: The subject must provide written informed consent prior to any study related procedures Women ≤50 years old BMI ≤ 25 kg/m2 Adequate endometrial thickness (>6.5mm) and pattern (Triple A structure) in the proliferative phase Exclusion Criteria: Uterine Pathology, adnexal pathology Systemic diseases -
Facility Information:
Facility Name
Ivi Valencia
City
Valencia
ZIP/Postal Code
46015
Country
Spain

12. IPD Sharing Statement

Learn more about this trial

Impact of Vaginal Microbiome on Vaginal Absorption of Exogenous Progesterone: a Pilot Study.

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