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Completed

NCT Number: NCT05473039

Effect of a Multivitamin Supplement With Probiotic (Seidivid Ferty4®) on Oocyte Retrieval and Quality

This study evaluates the effect of pretreatment with a multivitamin supplement with probiotics (Seidivid Ferty4®) on oocyte retrieval in normo-responder patients undergoing controlled ovarian hyperstimulation (COH) for oocyte donation, considering both the total number of oocytes retrieved and the number of mature oocytes retrieved, that is, in metaphase II (MII).

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Key information

Age range

18 year–34 year

Sex eligibility

Female

Study type

Interventional

Phase

Not applicable

Primary location

NextFertility

Valencia, 46009, Spain

About this study

Patients will be recruited on the day they are going to start the egg donation program. The patient will start taking the study treatment (multivitamin supplement with probiotics or placebo) immediately after inclusion and will call the site to initiate the oocyte donation protocol approximately 30 days after enrollment. Throughout the COH period of the protocol the patient will continue taking the study supplement (or placebo), without interruption until the day of the GnRH-agonist trigger. The administration of the agonist will be as a single dose, 36 hours before follicular puncture for the retrieval of mature eggs. Then, the retrieved oocytes will be denuded and examined by light microscopy to assess their quality. The evaluation will carried out by two different embryologists, blinded to the study protocol.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Women undergoing COH for egg donation cycles
  • Signing of Informed Consent
  • Age 18-34 years
  • Body mass index between 18-29.9 kg/m2
  • Meet the criteria for inclusion in the oocyte donation program of the Next Fertility center
  • Ultrasound antral follicle count before COH of ≥15 follicles

Exclusion criteria

  • Patients excluded from the oocyte donation program
  • Untreated sexually transmitted disease, HIV, HCV, HBV positive serology
  • Blood disorders, neurodegenerative/psychiatric diseases, fragile X syndrome, oncological diseases, endometriosis.
  • Polycystic ovary syndrome
  • Oligomenorrhea (<1 menstrual cycle in 3 months)
  • Diabetic patients

Treatment and study plan

Seidivid Ferty4

Dietary Supplement

The patient will start taking the study treatment (multivitamin supplement with probiotics) immediately after inclusion. Throughout the COH period of the protocol (usual mean duration: 11 days) the patient will continue taking the diatary supplement, without interruption until the day of the GnRH-agonist trigger.

Placebo

Other

The patient will start taking the study treatment (placebo) immediately after inclusion. Throughout the COH period of the protocol (usual mean duration: 11 days) the patient will continue taking the treatment (placebo), without interruption until the day of the GnRH-agonist trigger.

Primary outcomes

  1. Number of Oocytes Retrieved

    Time frame: Through study completion, an average of 42 days

    Total number of oocytes retrieved in the follicular puncture

  2. Number of Mature (MII) Oocytes Retrieved

    Time frame: Through study completion, an average of 42 days

    Total number of mature oocytes (metaphase II, or MII) retrieved in the follicular puncture

Secondary outcomes

  1. Number of Good Quality Oocytes

    Time frame: Through study completion, an average of 42 days

    Number of oocytes MII without dimorphisms

  2. Number of Oocytes With Dimorphisms

    Time frame: Through study completion, an average of 42 days

    Number of mature oocytes MII with dimorphisms

  3. Number of Follicles at the Time of Trigger Administration

    Time frame: Through trigger administration, an average of 40 days

    Ultrasound follicle count at the time of trigger administration

  4. Fasting Glucose After 30 Days of Treatment With Dietary Supplement.

    Time frame: Through COH start, an average of 30 days

    Fasting blood glucose at the start of controlled ovarian hyperstimulation (COH)

  5. AST After 30 Days of Treatment With Dietary Supplement.

    Time frame: Through COH start, an average of 30 days

    Serum aspartate aminotransferase (AST) levels at the time of controlled ovarian hyperstimulation (COH) start

  6. ALT After 30 Days of Treatment With Dietary Supplement.

    Time frame: Through COH start, an average of 30 days

    Serum alanine aminotransferase (ALT) levels at the time of controlled ovarian hyperstimulation (COH) start

  7. Cholesterol After 30 Days of Treatment With Dietary Supplement.

    Time frame: Through COH start, an average of 30 days

    Total cholesterol at the time of controlled ovarian hyperstimulation (COH) start

  8. LH at the Time of COH Start

    Time frame: Through COH start, an average of 30 days

    Plasma levels of luteinizing hormone (LH) at the time of controlled ovarian hyperstimulation (COH) start

Sponsors and collaborators

Lead sponsor

SEID S.A.

Industry

Registry information

Official study title

OvoVid Study: Effect of a Multivitamin Supplement With Probiotic (Seidivid Ferty4®) on Oocyte Retrieval and Quality in Oocyte Donors. Double-blind Randomized Placebo-controlled Clinical Trial

Acronym: OvoVid

Important dates

Study start
2022
Primary completion
2024
Study completion
2024
First posted
Jul 25, 2022
Registry last updated
Aug 13, 2025

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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