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

Sponsor
Instituto Valenciano de Infertilidad, IVI VALENCIA (Other)
Overall Status
Recruiting
CT.gov ID
NCT05161338
Collaborator
(none)
100
1
1
17.5
5.7

Study Details

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.

Condition or Disease Intervention/Treatment Phase
  • Diagnostic Test: MICROBIOME GENETIC ANALYSIS
  • Diagnostic Test: VAGINAL PH VALUE
  • Diagnostic Test: SERUM PROGESTERONE LEVELS
  • Diagnostic Test: SERUM OESTRADIOL LEVELS
N/A

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.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
100 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Intervention Model Description:
Prospective cohort unicentric pilot studyProspective cohort unicentric pilot study
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Impact of Vaginal Microbiome on Vaginal Absorption of Exogenous Progesterone: a Pilot Study.
Actual Study Start Date :
Feb 15, 2022
Anticipated Primary Completion Date :
Jan 1, 2023
Anticipated Study Completion Date :
Aug 1, 2023

Arms and Interventions

Arm Intervention/Treatment
Experimental: FROZEN EMBRYO TRANSFER

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

Diagnostic Test: MICROBIOME GENETIC ANALYSIS
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

Diagnostic Test: VAGINAL PH VALUE
Intravaginal Ph value meassurement.

Diagnostic Test: SERUM PROGESTERONE LEVELS
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-.

Diagnostic Test: SERUM OESTRADIOL LEVELS
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.

Outcome Measures

Primary Outcome Measures

  1. Vaginal Microbiome [12 months]

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

Secondary Outcome Measures

  1. Live birth [12 months]

    Live birth rate

  2. Ongoing Pregnancy Rate [12 months]

    Success value in pregnancy after ultrasound confirmation of heartbeat and 12 weeks of pregnancy

  3. Clinical Pregnancy [12 months]

    Pregnancy confirmation by the observation of the presence of at least one gestational sac on ultrasound

  4. Serum progesterone value [12 months]

    Serum progesterone levels

  5. Vaginal PH [12 months]

    Measure of vaginal pH levels

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 50 Years
Sexes Eligible for Study:
Female
Accepts Healthy Volunteers:
No
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 -

Contacts and Locations

Locations

Site City State Country Postal Code
1 Ivi Valencia Valencia Spain 46015

Sponsors and Collaborators

  • Instituto Valenciano de Infertilidad, IVI VALENCIA

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Instituto Valenciano de Infertilidad, IVI VALENCIA
ClinicalTrials.gov Identifier:
NCT05161338
Other Study ID Numbers:
  • 2110-VLC-095-EL
First Posted:
Dec 17, 2021
Last Update Posted:
Apr 7, 2022
Last Verified:
Mar 1, 2022
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Instituto Valenciano de Infertilidad, IVI VALENCIA
Additional relevant MeSH terms:

Study Results

No Results Posted as of Apr 7, 2022