NextFertility
Valencia, 46009, Spain
NCT Number: NCT05473039
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).
Looking for future studies?
Notify Me18 year–34 year
Female
Interventional
Not applicable
Valencia, 46009, Spain
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.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
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.
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.
Time frame: Through study completion, an average of 42 days
Total number of oocytes retrieved in the follicular puncture
Time frame: Through study completion, an average of 42 days
Total number of mature oocytes (metaphase II, or MII) retrieved in the follicular puncture
Time frame: Through study completion, an average of 42 days
Number of oocytes MII without dimorphisms
Time frame: Through study completion, an average of 42 days
Number of mature oocytes MII with dimorphisms
Time frame: Through trigger administration, an average of 40 days
Ultrasound follicle count at the time of trigger administration
Time frame: Through COH start, an average of 30 days
Fasting blood glucose at the start of controlled ovarian hyperstimulation (COH)
Time frame: Through COH start, an average of 30 days
Serum aspartate aminotransferase (AST) levels at the time of controlled ovarian hyperstimulation (COH) start
Time frame: Through COH start, an average of 30 days
Serum alanine aminotransferase (ALT) levels at the time of controlled ovarian hyperstimulation (COH) start
Time frame: Through COH start, an average of 30 days
Total cholesterol at the time of controlled ovarian hyperstimulation (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
SEID S.A.
Industry
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
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.
Published trials that share one or more normalized conditions with this study.
NCT07383480
Artificial Intelligence, Behavior
Clermont-Ferrand, France
View Trial DetailsNCT06773572
Behavior, Female Urogenital Diseases
Caracas, Venezuela
View Trial DetailsNCT04549649
Behavior, Helping Behavior
Tehran, Iran
View Trial DetailsNCT04458454
Behavior, Genital Diseases
Saint Petersburg, Russia
View Trial Details