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InfertilityNCT01408433

Single Embryo Transfer of a Euploid Embryo Versus Double Embryo Transfer

A study testing Single Embryo Transfer and Double embryo transfer in people with Infertility, run by Reproductive Medicine Associates of New Jersey at 2 sites 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

This study seeks to compare the pregnancy and delivery rates of patients who undergo a single embryo transfer, when the embryo has been tested and determined to be chromosomally normal, with pregnancy and delivery rates of patients who undergo a two (2) embryo transfer of untested embryos. Read more about this study

Who is it for?
Ages 18 to 43 yearsHealthy volunteers can take part
Conditions the study is for
Infertility
What is being tested?
Single Embryo Transfer and Double embryo transfer
Could I receive a placebo?
No, everyone receives an active treatment
How many people
175 participants
Where
2 sitesUnited States
Study dates
Aug 2011to Dec 2014
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 43 years
  • All sexes
  • Healthy volunteers accepted
  • Adult

Who may be able to join

  • Maximum of one (1) prior failed IVF cycle (a failed cycle is any cycle that did not deliver. Pregnancy losses are failed cycles. Ok to participate as a recipient in an egg donor cycle.)
  • Female partner less than 43 years old at time of onset of IVF cycle
  • Maximum prior day 3 follicle stimulation hormone (FSH) level of 12 (in RMA NJ laboratory)
  • Minimum anti-mullerian hormone (AMH)of 1.2 within 1 year
  • Normal uterine cavity demonstrated by saline sonogram, hysterosalpingogram or hysteroscopy within 1 year.
  • Male partner with greater than 100,000 total motile spermatozoa. Donor sperm ok.
  • Body Mass Index (BMI) less than or equal to 30 kg/m2.

Who cannot join

  • Diagnosis of chronic anovulation (cycles typically longer than 90 days)
  • Diagnosis of endometrial insufficiency- prior cycle with endometrial thickness less than 6mm, abnormal endometrial echotexture, persistent endometrial fluid.
  • Clinical indication of aneuploidy screening (i.e. history of loss of chromosomally abnormal pregnancies)
  • Clinical indication for PGD for single-gene disorder (i.e. PGD is needed to select against the transfer of embryos affected with a specific condition)
  • Use of testicular aspiration or biopsy procedures to obtain sperm
  • Unevaluated ovarian mass or surgically confirmed stage IV endometriosis
  • Presence of hydrosalpinges which communicate with the endometrial cavity
  • Any contraindication to undergoing in vitro fertilization

Trial locations and contacts

2 sites in 1 country.

United States2 sites
  • Reproductive Medicine Associated of Pennsylvania at lehigh Valley

    Allentown, Pennsylvania, 18104

  • Reproductive Medicine Associated of New Jersey

    Morristown, New Jersey, 07960

Other trials in United States

About this study

Official title: Single Embryo Transfer of a Euploid Embryo Versus Double Embryo Transfer: A Randomized Controlled Trial

This study seeks to compare the pregnancy and delivery rates of patients who undergo a single embryo transfer, when the embryo has been tested and determined to be chromosomally normal, with pregnancy and delivery rates of patients who undergo a two (2) embryo transfer of untested embryos.

Read the detailed description

This study will recruit patients from the NJ/NY/CT/eastern PA area only.

Twin and higher-order multiple pregnancies are the most common and most significant complication of pregnancies conceived through assisted reproductive technologies (ART). Twin rates in in vitro fertilization (IVF) cycles are approximately 30%. These pregnancies have increased complications for both the mother and the babies. A singleton, one baby, is the safest outcome for an IVF cycle. The surest way to reduce the risk of multiple births in IVF cycles is to transfer fewer embryos. Prior studies on single embryo transfer (SET) have shown decreased pregnancy rates because of the difficulty in selecting which embryo to transfer. Being chromosomally normal is necessary for the delivery of a healthy baby. The investigators are now able to screen all 24 chromosomes of an embryo with greater than 97% accuracy within four hours, allowing for a fresh embryo transfer of a tested embryo, using Comprehensive Chromosome Screening (CCS). This study seeks to show that the transfer of a single CCS-normal embryo will result in delivery rates equal to those resulting from a two embryo transfer, the current standard of care in IVF.

Patients will undergo IVF according to the protocol recommended by their primary doctor. On the day of egg retrieval, all mature eggs will be fertilized by intracytoplasmic sperm injection (ICSI) per routine laboratory protocol. Embryos will then be cultured out to day 5 per routine laboratory procedure. The embryos will be assessed by the embryologist on day 5 to determine if the patient is a candidate for a fresh transfer. Patients who are a candidate for fresh transfer will be randomized into either the single embryo transfer of a chromosomally normal embryo group or the double, untested embryo group. Patients will have a 50:50 chance of being in the single or double embryo transfer group. Embryos in the single embryo group will undergo biopsy for CCS and patients will then undergo transfer of the morphologically best, chromosomally normal embryo. Additional embryos will be cryopreserved. Patients in the double embryo transfer group will undergo a two embryo transfer. Additional embryos will be cryopreserved. If patients are not a candidate for a fresh transfer (potentially because of endometrial lining development, risk of ovarian hyperstimulation syndrome, or embryos that are not suitable for biopsy on day 5), they will still be randomized into either the single or double embryo transfer group. Patients in the single embryo transfer group will have all embryos biopsied for CCS prior to being frozen. Patients will then immediately undergo a synthetic frozen embryo transfer cycle in accordance with their randomization. Patients in the double embryo transfer group will have their embryos frozen and will then immediately prepare for a synthetic frozen embryo transfer cycle in accordance with their randomization. Any patient who does not become pregnant during their fresh transfer cycle will immediately undergo a synthetic frozen embryo transfer cycle in accordance with their original randomization.

All clinical follow up will be per routine regarding pregnancy testing, early pregnancy monitoring and subsequent transfer of care to the patient's obstetrician. If clinical miscarriage occurs, cells from the products of conception will be collected, if possible, and submitted for genetic analysis. If the pregnancy progresses to delivery, a buccal swab (small swab touched to the inside of the baby's cheek) will be collected and submitted for genetic analysis.

Conditions
Infertility
Being tested
Single Embryo Transfer, Double embryo transfer
Keywords
embryo transfer, in-vitro fertilization (IVF), pre-implantation diagnosis (PGD), infertility, single embryo transfer, two embryo transfer, double embryo transfer
Medical subject headings
Infertility

What participants receive

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

  • Single Embryo TransferOther

    Also called pre-implantation genetic diagnosis (PGD), in-vitro fertilization (IVF)

    single embryo transfer of a chromosomally normal embryo

  • Double embryo transferOther

    Also called two embryo transfer, in-vitro fertilization (IVF)

    two (2) embryo transfer of untested embryos

Study groups in NCT01408433
Study groupRoleWhat they receive
Single Embryo TransferOtherPatients will have a single, chromosomally normal embryo transferred.
Receives: Other: Single Embryo Transfer
Double Embryo TransferOtherPatients will have two (2) untested embryos transferred.
Receives: Other: Double embryo transfer

What is being measured

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

  1. Live birth rate per randomized patient (single embryo transfer vs. 2 embryo transfer)

    Compare live birth rates of patients who have a single embryo transfer of a chromosomally normal embryo with the live birth rates of patients who have two, untested embyros transferred.

    Measured: 2 years

Secondary outcomes (3)
  1. Twin live birth rate

    Compare twin live birth rates of patients who have a single embryo transfer of a chromosomally normal embryo with the twin live birth rates of patients who have two, untested embryos transferred.

    Measured: 2 years

  2. Sustained implantation rate (number of viable fetuses beyond the first trimester per embryo transferred)

    Compare sustained implantation rates of patients who have a single embryo transfer of a chromosomally normal embryo with the sustained implantation rates of patients who have two, untested embryos transferred.

    Measured: 2 years

  3. Live birth rate per embryo transfer

    Compare live birth rates per transfer of patients who have a single embryo transfer of a chromosomally normal embryo with the live birth rates per transfer of patients who have two, untested embryos transferred.

    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 posted3 Aug 2011 (estimated)
  2. Study startAug 2011
  3. Primary completionJul 2013
  4. Study completionDec 2014

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
Allocation
Randomised
Intervention model
Parallel groups
Masking
None (open label)
Enrolment
175 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT01408433
Sponsor's protocol ID
RMA-2011-01
Status last verified
Mar 2015
First submitted
1 Aug 2011
Last updated
26 Mar 2015
Results posted
No
Data monitoring committee
No

Publications

  • Forman EJ, Hong KH, Ferry KM, Tao X, Taylor D, Levy B, Treff NR, Scott RT Jr. In vitro fertilization with single euploid blastocyst transfer: a randomized controlled trial. Fertil Steril. 2013 Jul;100(1):100-7.e1. doi: 10.1016/j.fertnstert.2013.02.056. Epub 2013 Mar 30.

    PubMed 23548942

Questions about this trial

What is this clinical trial studying?

A study testing Single Embryo Transfer and Double embryo transfer in people with Infertility, run by Reproductive Medicine Associates of New Jersey at 2 sites 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 7 inclusion and 8 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 26 Mar 2015. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 2 sites 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 rate per randomized patient (single embryo transfer vs. 2 embryo transfer) (time frame: 2 years). 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 NCT01408433, which also lists 1 linked publication.

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 26 Mar 2015.

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