RecruitingNot ApplicableNCT06122207

Effect of a Probiotic on the Female Genital Tract Microbiota of Participants With Fertility Disorders.

A Randomized, Double-blind, Placebo-controlled Study to Confirm the Positive Effect of Fertibiome® (Ligilactobacillus Salivarius PS11610) on the Female Genital Tract Microbiota of Couples or Women With Fertility Disorders.


Sponsor

ProbiSearch SL

Enrollment

120 participants

Start Date

Feb 14, 2024

Study Type

INTERVENTIONAL

Conditions

Summary

In the last decades, numerous publications have broken the old paradigm that considered the urogenital tracts as sterile, demonstrating that microorganisms present in the urogenital tract represent the 9% of the whole human microbiome. Healthy urogenital microbiome improves implantation rate and pregnancy outcomes, whereas 40% of dysbiosis prevalence is observed in women under assisted reproductive treatment (ART). Infertility causes are associated with male, female, or combined failure. It has been shown that oral probiotic treatment, mainly with Lactobacillus, recovers a healthy vaginal microbiota without safety concerns. An interventional, randomized, double-blind, placebo-controlled study will be conducted to confirm the positive effect of the commercial probiotic product Fertibiome® on the vaginal dysbiosis of couples or women with fertility disorders. The duration of the study will be of 6 months approximately, including 6 months of product intake. In case of pregnancy during intervention, women will continue their participation until week 12 of gestation. Participants will be randomly assigned to one of the two study groups: control group with placebo administration or probiotic administration group. Women will take 1 capsule every 12 hours and men 1 per day. In case of women participating alone they will take 1 capsule every 12 hours. In case of pregnancy, only women will continue taking 1 capsule per day for the first 12 weeks.


Eligibility

Min Age: 18 YearsMax Age: 40 Years

Inclusion Criteria4

  • Couples or women with ages between 18 and 40 for woman and between 18 and 55 for man (in case of couple participation).
  • Couples or women with fertility disorders.
  • Couples or women undergoing IVF treatment or willing to start it.
  • Signature of the Informed Consent.

Exclusion Criteria13

  • Women, not participating in the study with a couple, who have not undergone at least 4 cycles of artificial insemination with donor's sperm (AID) or 1 cycle of IVF without achieving evolutionary pregnancy.
  • Women with Body Mass Index (BMI) ≥ 30.
  • Couples where the woman has not infertility diagnosis while the man has any of the following characteristics:
  • Azoospermia
  • Sperm motility (A + B) < 25%.
  • Sperm morphology ≤ 2%.
  • Vas deferens obstruction.
  • Couples or women with any of the following characteristics:
  • Chronic diseases that cause intestinal malabsortion.
  • Congenital or acquired immunodeficiency.
  • Current history or diagnosis of alcohol, tobacco, or drug abuse.
  • Uncertainty about the willingness or ability of participants to comply with the requirements of the protocol.
  • Under treatment with probiotics during the last week.

Interested in this trial?

Get notified about updates and connect with the research team.

Interventions

DIETARY_SUPPLEMENTProbiotic

* Women: 1 capsule of probiotic (Ligilactobacillus salivarius PS11610) every 12 hours for 6-months. In case of pregnancy: * Women: 1 capsule of probiotic per day for 12 weeks. * Men: 1 capsule of probiotic (Ligilactobacillus salivarius PS11610) per day for 6-months.

DIETARY_SUPPLEMENTPlacebo

* Women: 1 capsule of placebo every 12 hours for 6-months. In case of pregnancy: * Women:1 capsule of placebo per day for 12 weeks. * Men: 1 capsule of placebo per day for 6-months.


Locations(2)

Dr. Miguel Raimundo (Portugal)

Lisbon, Portugal

Hospital Universitario La Paz

Madrid, Madrid, Spain

View Full Details on ClinicalTrials.gov

For the most up-to-date information, visit the official listing.

Visit

NCT06122207


Related Trials