ClinicalTrials.Veeva

Menu

Evolutive Potential of Embryos Obtained From Oocytes After Luteal Phase Ovarian Stimulation

I

Institut Universitari Dexeus

Status

Completed

Conditions

Ovulation Induction
Vitrification
INFERTILITY
Fertility Preservation
Oocyte Donation

Treatments

Drug: ganirelix
Drug: gonadotropins plus GnRH antagonists

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

The purpose of this study is to evaluate the clinical pregnancy rate per embryo transfer in oocytes recipients obtained after ovarian stimulation during the luteal phase of oocytes donors . This study will be performed in egg recipients and donors but this type of treatment is meant to be implemented in fertility preservation patients

Enrollment

15 patients

Sex

Female

Ages

18 to 35 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • premenopausal women, 18-35 years old, FSH levels < 10 mIU/ml; AFC> 10
  • regular cycles
  • BMI < 28
  • signed informed consent

Recipients:

  • Infertile women eligible for oocytes donation
  • BMI < 35
  • Signed informed consent form

Exclusion criteria

-Polycystic ovarian syndrome, gonadotropins allergy

Recipients:

  • Women eligible for oocytes donation
  • BMI >35
  • Uncontrolled Endocrine Pathology

Trial design

Primary purpose

Treatment

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

15 participants in 1 patient group

Lutheal phase ovarian stimulation
Experimental group
Description:
Early luteal phase Controlled ovarian hyperstimulation: we will administer in the 13th-15th cycle day simultaneously 0.25 mg/day of ganirelix to induce luteolysis and FSHr (dose according to BMI and AFC )IU/day for controlled ovarian hyperstimulation until achieving criteria for hCG , to induce final oocyte maturation. Mature oocytes will be vitrified. After warming, oocytes will be inseminated by ICSI with the recipients partners semen sample . Recipient endometrium will be primed with estrogen and progesterone , and embryo transfer will be performed on the 3rd day 3 of embryo cleavage.
Treatment:
Drug: gonadotropins plus GnRH antagonists
Drug: ganirelix

Trial contacts and locations

1

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems