Impact of Corpus Luteum Presence or Absence in the Incidence of Preeclampsia After Frozen Embryo Transfer

NCT ID: NCT04092829

Last Updated: 2024-03-22

Basic Information

• Recruitment Status: TERMINATED
• Clinical Phase: NA
• Total Enrollment: 591 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2019-09-16
• Study Completion Date: 2022-12-31

Brief Summary

Identifying modifiable factors that contribute to preeclampsia risk associated with assisted reproduction can improve maternal health. Recent studies have shown an increased risk for hypertensive disorders of pregnancy after in vitro fertilization, particularly for pregnancies occurring during a hormone replacement therapy such a donor egg recipient and a frozen embryo transfer. This risk may be partly attributable to the degree by which the assisted reproductive treatment affects the maternal hormonal environment, when the corpus luteum is a major source of reproductive hormones. On the other hand, cryopreserved embryos are usually thawed and replaced in in a natural or hormonally manipulated cycle; on this point, frozen embryo transfer is associated with better perinatal outcome regarding preterm birth and low birth weight yet higher risk of large for gestational age and macrosomia compared to fresh transfer. The objective of our study is to investigate whether the absence of corpus luteum adversely affects pregnancy and to analyse if there are differences in the perinatal outcomes due to differences in the endometrial preparation protocol for a frozen embryo transfer.

Conditions

Pre-Eclampsia; Frozen Embryo Transfer

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: DIAGNOSTIC
• Blinding Strategy: NONE

Study Groups

FROZEN EMBRYO TRANSFER IN NATURAL CYCLE

After confirming ovarian rest (follicles \< 10 mm) with menstruation by means of vaginal ultrasound, an ultrasound control of the natural cycle will be carried out, inducing ovulation when an ovulatory follicle of size ≥ 17mm and an endometrium ≥ 7mm are found. Serum estradiol and progesterone values will be determined that day. This induction will be carried out with an ampoule of 250 μg of rHCG (Ovitrelle®). After the injection of Ovitrelle®, the administration of micronized vaginal progesterone (Progeffik® or Utrogestan®) 200 mg/ 12 hours and 7 days after the injection, thawing and transfer of a frozen euploid blastocyst will begin 48 hours later.

Group Type: NO_INTERVENTION

No interventions assigned to this group

FROZEN EMBRYO TRANSFER IN SUBSTITUTED CYCLE

After confirming ovarian rest (follicles \< 10 mm) with menstruation by vaginal ultrasound, hormone replacement therapy with oestrogens (6 mg/day of oral oestradiol valerate - Progynova® or Progyluton®- or 150 ug/48 h of oestradiol in patches - Evopad®) will be started on day 2-3 of the cycle. On day 10-15 of treatment an ultrasound scan will be performed to assess endometrial growth and ovarian rest. After confirming an endometrial thickness ≥ 7mm by vaginal ultrasound, ovaries with follicles smaller than 10 mm, blood estradiol \>100 pg/ml and serum progesterone \< 1 ng/ml, luteal phase support will begin with the administration of 400 mg of micronized vaginal progesterone every 12 hours, a total of 10 shots, prior to embryo transfer of a thawed euploid blastocyst. same day. If the level of serum progesterone on the day of transfer is less than 9.2 ng/ml, a daily injection of subcutaneous progesterone (Prolutex®) will be added on the same day.

Group Type: ACTIVE_COMPARATOR

FROZEN EMBRYO TRANSFER IN SUBSTITUTED CYCLE

Intervention Type: PROCEDURE

The intervention group will be prepared with hormone replacement therapy with estrogens according to usual clinical practice. Frozen embryos will be transferred after ten doses of exogenous progesterone.

Interventions

FROZEN EMBRYO TRANSFER IN SUBSTITUTED CYCLE

The intervention group will be prepared with hormone replacement therapy with estrogens according to usual clinical practice. Frozen embryos will be transferred after ten doses of exogenous progesterone.

Intervention Type: PROCEDURE

Eligibility Criteria

Inclusion Criteria

• All patients who, after IVF-PGT-A treatment with their own oocytes, present a euploid embryo for transfer.
• Transfer of a single euploid embryo

Exclusion Criteria

• Moderate or high smoking (> 5 cigarettes/day)
• BMI ≥30 kg/m2
• Chronic hypertension
• History of preeclampsia in previous pregnancies
• History of delayed uterine growth and placental insufficiency in previous pregnancies
• Use of donor sperm
• Woman's age ≥44 years
• Women with menstrual cycles longer than 35 days

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 44 Years
• Eligible Sex: FEMALE
• Accepts Healthy Volunteers: No

Sponsors

IVI Bilbao

OTHER

Sponsor Role: collaborator

IVI Barcelona

OTHER

Sponsor Role: collaborator

IVI Madrid

OTHER

Sponsor Role: collaborator

Vida Recoletas Sevilla

OTHER

Sponsor Role: collaborator

IVI Vigo

OTHER

Sponsor Role: collaborator

IVI Roma

OTHER

Sponsor Role: collaborator

Hospital Universitario La Paz

OTHER

Sponsor Role: collaborator

IVI Mallorca

NETWORK

Sponsor Role: collaborator

Instituto Valenciano de Infertilidad, IVI VALENCIA

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

JOSE BELLVER PRADAS, MDPhD

Role: PRINCIPAL_INVESTIGATOR

IVIRMA VALENCIA

Locations

Ivi Valencia

Valencia, , Spain

Countries

Spain

Other Identifiers

1906-VLC-067-JB

Identifier Type: -

Identifier Source: org_study_id