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InfertilityPRECiSENCT03764865

PooR Embryo Yield Cleavage Stage Versus blaStocyst Embryo Transfer (PILOT STUDY)

A study testing day 3 uterine transfer and day 5 uterine transfer in people with Infertility, run by Beth Israel Deaconess Medical Center at 1 site in United States.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

The purpose of this small-scale pilot study (10 patients) is to test the study protocol for an RCT comparing IVF outcomes between day 3 and day 5 embryo transfer in patients with five or fewer embryos in a fresh embryo transfer in vitro fertilization (IVF) cycle. Read more about this study

Who is it for?
Ages 18 to 44 years, women only
Conditions the study is for
Infertility
What is being tested?
day 3 uterine transfer and day 5 uterine transfer
Type of treatment
Surgery or procedure
Could I receive a placebo?
No, everyone receives an active treatment
How many people
10 participants
Where
1 siteUnited States
Study dates
1 Mar 2021to 28 Feb 2022
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 44 years
  • Women only
  • No healthy volunteers
  • Adult

Who may be able to join

  • First autologous IVF cycle
  • Written, informed consent

Who cannot join

  • Planned gestational carrier
  • Planned donor egg
  • Morbid obesity: BMI >40
  • History of recurrent pregnancy loss (≥2 spontaneous abortions)
  • Presence of uterine factor infertility
  • Treatment plan includes embryos cultured 'out of protocol'
  • Planned preimplantation genetic testing

Trial locations and contacts

1 site in 1 country.

United States1 site
  • Boston IVF

    Waltham, Massachusetts, 02451

Other trials in United States

About this study

Official title: Day 3 vs Day 5 Embryo Transfer for Patients With Low Embryo Numbers Going Through in Vitro Fertilization (PILOT STUDY)

The purpose of this small-scale pilot study (10 patients) is to test the study protocol for an RCT comparing IVF outcomes between day 3 and day 5 embryo transfer in patients with five or fewer embryos in a fresh embryo transfer in vitro fertilization (IVF) cycle. Information derived from this RCT would allow us to maximize the chances of success for these patients undergoing IVF.

Read the detailed description

Embryos created with assisted reproductive technology (ART, e.g. in vitro fertilization (IVF)) are commonly transferred into a woman's uterus at either the cleavage stage (day 3 after egg retrieval) or blastocyst stage (day 5 after egg retrieval). Until recently, most IVF cycles transferred embryos at the cleavage stage. However, with improvements in in vitro culture technique there has been a steady shift in practice to transfer embryos at the blastocyst stage (day 5 after egg retrieval) as this timing is about the same as when embryos reach the endometrial cavity in natural conception.

There now is a general consensus that, for good prognosis patients, those with a high embryo from the IVF cycle, it is beneficial to transfer the embryo on day 5 rather than day 3. The rationale for this is to allow for self-selection of embryos, meaning those that develop to blastocyst in vitro are more likely to be viable in vivo and result in a viable pregnancy. In addition, transferring an embryo on day 5 improves uterine/embryonic synchronicity and thereby improves outcomes. This allows the transfer of fewer embryos and decreases the likelihood of multiples (twins, triplets, etc.).

As a result, day 5 transfer has become standard of care for good prognosis patients in the United States. The American Society of Reproductive Medicine1 issued a committee opinion in 2013 to this effect stating that in "good prognosis" patients, blastocyst transfer results in a significant increase in live birth rates compared to transfer of an equal number of cleavage stage embryos (50.5% vs. 30.1%, P< .01)2-5. In addition, for unselected and poor prognosis patients, no high-quality studies have evaluated whether blastocyst transfer increases live birth rates when compared to cleavage stage transfer.

It is possible that the attrition of day 3 embryos in vivo is lower than the attrition in vitro and that day 5 transfer leads to loss of embryos that may have survived in vivo. In addition, women undergoing blastocyst culture are expected to have a higher incidence of cycle cancellation due to failure of the embryo to develop to a blastocyst6 and of having fewer embryos cryopreserved (frozen)7. Because of this, in Europe and Asia, day 3 transfer is the most common practice.

On the other hand, transferring embryos on day 3 decreases our ability to select the best embryo, increases laboratory costs and may increase multiple pregnancy rates as, typically, more embryos are transferred at this time. In addition, in vivo, day 3 embryos are in transit through the fallopian tube during natural conception and are exposed to a different developmental and nutritional environment than day 3 IVF embryos transferred into the uterine cavity. Thus, it is possible that exposing day 3 embryos to the physiologically premature uterine environment (particularly one that has been subjected to superovulation and thus high levels of estrogen) increases embryo attrition compared to day 5 transfer, particularly in poor prognosis patients.

Therefore, a clinical dilemma exists for poor prognosis patients (those with ≤5 embryos available on day 1 after egg retrieval). Currently, many practices in the United States transfer embryos from these patients on day 3 due to the risk of not having embryos available to transfer on day 5. Any remaining embryos are then frozen if they meet criteria on day 5/6.

Retrospective data from Boston IVF, BIDMC's affiliated infertility treatment center, demonstrates that the live birth rate per transfer among poor prognosis patients is 18% among those who have a cleavage stage transfer and 38% among those who have a blastocyst transfer.

At Boston IVF, about 35% of patients have a day 3 embryo transfer, which is consistent with national trends. For a patient undergoing an IVF cycle at Boston IVF, a physician may choose to transfer an embryo on day 3 or day 5 or allow the laboratory to make that decision, based on the number of embryos the patient has on day 1 after egg retrieval and the patient's age. This decision typically is made prior to the IVF cycle. As demonstrated above, pregnancy rates are far lower in the cleavage stage transfer group and there is the possibility that, within a select cohort of these patients, we are unrealistically raising patient's expectations of a live birth.

The purpose of this study is to compare IVF outcomes among poor prognosis patients (≤5 embryos with two pronuclei) who have a day 3 transfer to those who have a day 5 transfer.

Conditions
Infertility
Being tested
day 3 uterine transfer, day 5 uterine transfer
Keywords
cleavage embryo, blastocyst, embryo transfer, in vitro fertilization
Medical subject headings
Infertility

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • day 3 uterine transferProcedure or surgery

    uterine transfer of embryo on day 3 after fertilization (cleavage stage)

  • day 5 uterine transferProcedure or surgery

    uterine transfer of embryo on day 5 after fertilization (blastocyst stage)

Study groups in NCT03764865
Study groupRoleWhat they receive
day 3 embryo transferExperimentalembryo transfer 3 days after fertilization
Receives: Procedure: day 3 uterine transfer
day 5 embryo transferExperimentalembryo transfer 5 days after fertilization
Receives: Procedure: day 5 uterine transfer

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. live birth

    defined as delivery of a live born infant ≥22 weeks of gestation

    Measured: 9 months

Secondary outcomes (4)
  1. Clinical pregnancy

    defined by confirmation of a gestational sac on ultrasound

    Measured: 14 days

  2. Ongoing pregnancy

    defined by ultrasound confirmation of a gestational sac with at least one fetal pole with a fetal heartbeat

    Measured: 9 months

  3. Multiple pregnancy

    defined as twins or higher-order gestations

    Measured: 9 months

  4. Time to pregnancy/live birth

    Measured: 2 years

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted5 Dec 2018
  2. Study start1 Mar 2021
  3. Primary completion28 Feb 2022
  4. Study completion28 Feb 2022

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Model description
non-inferiority
Masking
None (open label)
Enrolment
10 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT03764865
Sponsor's protocol ID
2018P000530
Acronym
PRECiSE
Status last verified
Nov 2023
First submitted
4 Dec 2018
Last updated
8 Nov 2023
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Publications

  • Practice Committees of the American Society for Reproductive Medicine and the Society for Assisted Reproductive Technology. Blastocyst culture and transfer in clinical-assisted reproduction: a committee opinion. Fertil Steril. 2013 Mar 1;99(3):667-72. doi: 10.1016/j.fertnstert.2013.01.087.

    PubMed 23714439
  • Gardner DK, Schoolcraft WB, Wagley L, Schlenker T, Stevens J, Hesla J. A prospective randomized trial of blastocyst culture and transfer in in-vitro fertilization. Hum Reprod. 1998 Dec;13(12):3434-40. doi: 10.1093/humrep/13.12.3434.

    PubMed 9886530
  • Glujovsky D, Farquhar C, Quinteiro Retamar AM, Alvarez Sedo CR, Blake D. Cleavage stage versus blastocyst stage embryo transfer in assisted reproductive technology. Cochrane Database Syst Rev. 2016 Jun 30;(6):CD002118. doi: 10.1002/14651858.CD002118.pub5.

    PubMed 27357126
  • Papanikolaou EG, D'haeseleer E, Verheyen G, Van de Velde H, Camus M, Van Steirteghem A, Devroey P, Tournaye H. Live birth rate is significantly higher after blastocyst transfer than after cleavage-stage embryo transfer when at least four embryos are available on day 3 of embryo culture. A randomized prospective study. Hum Reprod. 2005 Nov;20(11):3198-203. doi: 10.1093/humrep/dei217. Epub 2005 Jul 29.

    PubMed 16055454
  • Papanikolaou EG, Camus M, Kolibianakis EM, Van Landuyt L, Van Steirteghem A, Devroey P. In vitro fertilization with single blastocyst-stage versus single cleavage-stage embryos. N Engl J Med. 2006 Mar 16;354(11):1139-46. doi: 10.1056/NEJMoa053524.

    PubMed 16540614
  • Marek D, Langley M, Gardner DK, Confer N, Doody KM, Doody KJ. Introduction of blastocyst culture and transfer for all patients in an in vitro fertilization program. Fertil Steril. 1999 Dec;72(6):1035-40. doi: 10.1016/s0015-0282(99)00409-4.

    PubMed 10593377
  • Tsirigotis M. Blastocyst stage transfer: pitfalls and benefits. Too soon to abandon current practice? Hum Reprod. 1998 Dec;13(12):3285-9. doi: 10.1093/humrep/13.12.3285. No abstract available.

    PubMed 9886498
  • Neuhausser WM, Vaughan DA, Sakkas D, Hacker MR, Toth T, Penzias A. Non-inferiority of cleavage-stage versus blastocyst-stage embryo transfer in poor prognosis IVF patients (PRECiSE trial): study protocol for a randomized controlled trial. Reprod Health. 2020 Jan 30;17(1):16. doi: 10.1186/s12978-020-0870-y.

    PubMed 32000803

Questions about this trial

What is this clinical trial studying?

A study testing day 3 uterine transfer and day 5 uterine transfer in people with Infertility, run by Beth Israel Deaconess Medical Center at 1 site in United States.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 2 inclusion and 7 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 8 Nov 2023. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in United States. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

live birth (time frame: 9 months). It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT03764865, which also lists 8 linked publications.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 8 Nov 2023.

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PRECiSE Clinical Trial NCT03764865 | AzTrials