Actively Recruiting

Phase 3
Age: 18Years - 44Years
FEMALE
ID06746129

Day 3 Versus Day 5 Embryo Transfer in IVF Patients With Few Embryos

Led by Beth Israel Deaconess Medical Center · Updated on 2026-04-02

1126

Participants Needed

1

Research Sites

30 weeks

Total Duration

On this page

Sponsors

B

Beth Israel Deaconess Medical Center

Lead Sponsor

B

Brigham and Women's Hospital

Collaborating Sponsor

AI-Summary

What this Trial Is About

Infertility affects over 6 million women in the United States and brings various emotional, physical, and financial challenges. This research aims to compare pregnancy outcomes and patient satisfaction between two embryo transfer timings in IVF patients who have five or fewer embryos. The study focuses on helping patients and providers make evidence-based decisions on when to transfer embryos to improve counseling and reduce anxiety, especially for those with a poor prognosis. The trial randomly assigns 1126 women aged 18 to 44 undergoing their first IVF cycle with five or fewer embryos to either receive embryo transfer at the cleavage stage (day 3, 8-cell embryo) or at the blastocyst stage (day 5-7 embryo). Surplus embryos that meet freezing criteria may be frozen and transferred in a later cycle. The study is conducted across nine IVF centers in the US. Participants will be monitored for six months or until all embryos have been transferred, and if pregnancy occurs, follow-up continues until delivery. Researchers will assess the chance of live birth per cycle, risks of miscarriage, multiple pregnancies, and cycle cancellations, along with secondary measures such as time to pregnancy, number of procedures, adverse perinatal outcomes, financial burden, and patient satisfaction. The study also examines factors affecting patient involvement in embryo transfer timing and guideline implementation.

CONDITIONS

Brief Title

Cleavage-stage Versus Blastocyst-stage Embryo Transfer in IVF Patients With Few Embryos

Who Can Participate

Age: 18Years - 44Years
FEMALE

Eligibility Criteria

Eligible

You may qualify if you...

  • Undergoing autologous IVF cycle
  • Have 5 or fewer zygotes on day 1 of embryo development
  • Planned fresh embryo transfer
Not Eligible

You will not qualify if you...

  • Planned preimplantation genetic testing (PGT) of all embryos
  • More than 2 previous IVF cycles
  • History of recurrent pregnancy loss (3 or more losses)
  • Body mass index (BMI) greater than 40
  • Uterine factor infertility
  • Planned gestational carrier
  • Endometrial lining less than 6mm on trigger day
  • Use of Lupron-only trigger or elevated progesterone in fresh cycle (≥1.5 ng/ml)
  • Delayed fertilization (more than 18 hours)
  • Rescue intracytoplasmic sperm injection after failed fertilization
  • Use of non-ejaculated sperm (testicular sperm extraction)
  • Embryo transfer number outside ASRM guidelines
  • Cycle converted to all embryos frozen

AI-Screening

AI-Powered Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Treatment

Duration - Up to 6 months or until all embryos are transferred

Participants receive embryo transfer either at the cleavage stage (day 3) or blastocyst stage (day 5-7) as part of their IVF treatment.

Visits aligned with embryo transfer procedures and monitoring during IVF cycles

Follow-up

Duration - Up to 9 months after embryo transfer until delivery

Participants are monitored for pregnancy outcomes including live birth, multiple pregnancy, and other pregnancy-related assessments until delivery if pregnancy is achieved.

Approximately monthly visits or contacts during pregnancy

Trial Site Locations

Total: 1 location

1

Boston IVF

Boston, Massachusetts, United States, 02451

Actively Recruiting

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Research Team

B

Beatrice Duvert

W

Werner Neuhausser, MD PhD

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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