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Administration of Human Chorionic Gonadotrophin Before Secretory Transformation of Frozen-thawed Embryo Transfer Cycles

A

Alexandria University

Status and phase

Completed
Phase 4

Conditions

Frozen-thawed Embryo Transfe
hCG
Human Chorionic Gonadotrophin
FET

Treatments

Drug: Human Chorionic Gonadotrophin Intramuscular injection 10.000 IU

Study type

Interventional

Funder types

Other

Identifiers

NCT05340010
HCG in FET cycles

Details and patient eligibility

About

Successful embryo implantation is complicated process that requires synchrony between good-quality embryos and receptive endometrium. Human chorionic gonadotropin (hCG), is one of the initial embryonic signals and the major embryoendometrial relationship regulator. This study will be conducted to to investigate the role of parenteral hCG used for the transfer of cryopreserved- thawed embryos with HRT cycles in the outcome of artificially prepared frozen embryo transfer (FET) cycles.

Enrollment

180 patients

Sex

Female

Ages

18 to 38 years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria:

  • Patient age ≤ 38 years.
  • Normal 3D transvaginal ultrasound.
  • At least two good quality embryos cryopreserved by vitrification.
  • No GnRH agonists administration before FET cycle.

Exclusion Criteria

  • Endometriosis.
  • Uterine anomalies.
  • Evidence of hydrosalpinx by hystrosalpingography or ultrasound.
  • Evidence of immune disease, hematological or hormonal disorder.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

180 participants in 2 patient groups

HCG group
Experimental group
Description:
n Group 1 (hCG): participants will receive endometrial preparation with estrogen and an intramuscular hCG injection will before progesterone supplementation
Treatment:
Drug: Human Chorionic Gonadotrophin Intramuscular injection 10.000 IU
control group
No Intervention group
Description:
Group 2 (control): participants will receive the conventional endometrial preparation with estrogen followed by progesterone supplementation

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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