Actively Recruiting
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
Eligibility Criteria
You may qualify if you...
- Undergoing autologous IVF cycle
- Have 5 or fewer zygotes on day 1 of embryo development
- Planned fresh embryo transfer
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
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
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
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
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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