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Recruiting

NCT Number: NCT07004192

The Role of hCG in Thawed Embryo Transfer

This prospective randomized trial will assess the relevance, if any, of a corpus luteum induced by hCG in transfers of thawed embryos.

Recruiting

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Key information

Age range

18 year and older

Sex eligibility

Female

Study type

Interventional

Phase

Phase 4

Primary location

Fertility Center of Las Vegas

Las Vegas, Nevada, 89113, United States

Location status: Recruiting

Location contact

Shironda Research Assistant

CONTACT

[email protected]

702-254-1777 ext. 265

About this study

The current study is designed to carefully isolate the effect of a corpus luteum by ensuring that the presence or absence of a corpus luteum is the only difference between two study arms. This should be reliably achieved by administering an injection of hCG in one study arm, while the other study arm has identical treatment except for omitting the hCG.

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

  • Female adult expecting to receive transfer of a thawed embryo.
  • At least one available frozen blastocyst of transferrable quality.
  • Non-menopausal female with at least one antral follicle.
  • Use of pre-implantation genetic testing (PGT), embryos derived from donor oocytes and/or donor sperm, a gestational carrier, and history of prior transfer(s) regardless of outcome are allowed.
  • Subsequent embryo transfers after failed transfers under this study are allowed, but not after a transfer that has resulted in ongoing pregnancy at ten weeks gestation under this study.

Exclusion criteria

  • Minors (age<18 years).
  • Use of embryo(s) frozen at another center.
  • Patient insistent on transfer of two embryos.
  • Patient or partner unable to provide informed consent in English.
  • Patient already enrolled in any other research study for her embryo transfer.
  • History of anti-phospholipid syndrome or any other indication for use of Lovenox in pregnancy.
  • Patient for whom the physician assesses this protocol is inappropriate or unsafe.

Treatment and study plan

HCG injection

Drug

5000 IU hCG injection

No intervention

Other

No hCG administered in this group.

Primary outcomes

  1. Blood pressure

    Time frame: Third trimester of pregnancy

    Mean arterial pressure measured in third trimester of pregnancy

Study contacts

Contact information is provided by the study sponsor or research team.

Shironda Research Assistant

CONTACT

[email protected]

702-254-1777 ext. 265

Sponsors and collaborators

Lead sponsor

Fertility Center of Las Vegas

Industry

Registry information

Important dates

Study start
2025
Primary completion
2027
Study completion
2027
First posted
Jun 4, 2025
Registry last updated
Jul 1, 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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