Embryo Freezing and Frozen Embryo Transfer (FET) Explained
Twenty years ago, freezing an embryo meant accepting a lower chance of it working. That is no longer true. A change in freezing technique has been one of the quietest but most significant advances in fertility medicine, and it has reshaped how IVF cycles are planned. Today a frozen embryo transfer is at least as successful as a fresh one in most situations, and in several specific circumstances it is clearly safer. This guide explains how embryo freezing works, what an FET cycle involves, and why your clinic may recommend freezing everything rather than transferring straight away.
Why Freezing Changed
The old method, slow freezing, lowered the temperature gradually. The problem was ice. Ice crystals forming inside cells damaged them, and a meaningful proportion of embryos did not survive thawing.
Vitrification replaced it. The embryo is exposed to a protective solution and then cooled so rapidly that water has no time to crystallise; it passes straight into a glass-like solid state. Survival rates after thawing are now very high, and the embryo that comes out is, for practical purposes, the embryo that went in.
"Freezing is no longer a compromise. In many cycles it is the better plan, chosen deliberately rather than as a fallback."
Why Embryos Are Frozen
Surplus good embryos from a fresh cycle. One stimulation and egg collection often produces more than one usable embryo. Freezing the rest means a second or third attempt without repeating the injections.
Freeze-all to avoid ovarian hyperstimulation. Where a woman has responded strongly, transferring in that cycle raises OHSS risk considerably. Freezing everything and transferring later removes that risk almost entirely. See IVF injections and their side effects.
A uterine lining that is not ready. High hormone levels during stimulation can make the endometrium less receptive. A later natural or prepared cycle gives a better lining.
Progesterone rising too early during stimulation, which shifts the implantation window out of step with the embryo.
Genetic testing of embryos, which requires time for results before transfer.
Fertility preservation before chemotherapy or radiotherapy. Our oncology department raises this with younger patients before treatment starts.
A medical or personal reason to delay, such as illness, surgery or travel.
Accumulating embryos across cycles where ovarian reserve is low, so that a transfer happens only once there is a reasonable number banked. See the AMH test and ovarian reserve.
Fresh Versus Frozen Transfer
Fresh transfer
Frozen transfer
Timing
3–5 days after egg collection, in the same cycle
In a later cycle, weeks or years afterwards
Hormone environment
High oestrogen from stimulation
Natural or carefully prepared
OHSS risk
Present, and increased by pregnancy
Effectively removed
Physical demand
Follows immediately on from collection
Body has recovered; no injections for stimulation
Scheduling
Fixed by the cycle
Flexible, easier to plan around work and travel
Success
Good
Equal or better in most groups, particularly strong responders
Fresh transfer remains appropriate for many patients, particularly those with a normal response and a good lining. The point is that neither is automatically superior; the choice should be made on your response in that specific cycle.
How a Frozen Embryo Transfer Cycle Runs
An FET cycle is considerably lighter than a stimulation cycle. There is no egg collection, no sedation and no ovarian stimulation.
Preparing the lining: two approaches
Natural cycle FET. Your own ovulation is tracked by ultrasound and blood tests, and the transfer is timed to it. Suitable for women with regular cycles, and uses minimal medication.
Hormone-prepared (medicated) FET. Oestrogen tablets or patches build the lining, then progesterone is added to open the implantation window. This gives precise control over timing and is used where cycles are irregular.
The sequence
Baseline scan at the start of the cycle.
Lining preparation over roughly two weeks, monitored by ultrasound for endometrial thickness and pattern.
Progesterone started once the lining is ready, which sets the transfer date.
Thawing on the morning of transfer, with the embryologist confirming survival before you proceed.
Transfer — a fine catheter passes through the cervix under ultrasound guidance. It takes a few minutes, needs no anaesthesia, and feels similar to a smear test.
Luteal support with progesterone, continuing until the pregnancy test and usually into early pregnancy.
Blood pregnancy test about ten to fourteen days later.
No bed rest is needed after transfer. Studies consistently show no benefit, and prolonged lying down may be marginally counterproductive. Return to normal light activity, avoid heavy lifting and very strenuous exercise, and continue your progesterone exactly as prescribed.
Common Questions About Storage
How long can embryos be stored? Vitrified embryos do not deteriorate measurably with time in storage. Healthy babies have been born from embryos frozen for many years. Storage duration is governed by national regulations and your clinic's consent forms rather than by biology.
Does freezing harm the embryo? Modern vitrification has high survival rates, and large studies have not shown an increase in birth defects in babies born from frozen embryos compared with fresh.
What if an embryo does not survive thawing? A small proportion do not. If you have more than one stored, another can usually be thawed the same day, which is one reason clinics discuss how many to bank.
What happens to embryos we do not use? You will be asked to record your wishes in writing in advance — continued storage, donation for research where permitted, or allowing them to perish. It is worth discussing this as a couple before you sign, not afterwards.
Are there storage fees? Yes, usually annual. Ask for the figure in writing at the outset and check what happens if a payment is missed.
Read the consent forms properly. Storage consent covers what happens to your embryos if you separate, if one partner dies, or if you lose contact with the clinic. These are uncomfortable questions and they are far easier to answer now than in the middle of a dispute later.
Frozen Transfer and Pregnancy Outcomes
Babies conceived from frozen embryos are, on average, slightly heavier at birth than those from fresh transfers, and the risk of low birth weight and preterm birth is somewhat lower. On the other side, medicated frozen cycles carry a slightly higher rate of hypertensive disorders in pregnancy, which is one reason natural-cycle FET is preferred where a woman ovulates regularly.
Yes, and in several groups it is better. Since vitrification replaced slow freezing, embryo survival after thawing is very high. Frozen transfer avoids the high oestrogen environment of a stimulation cycle, which can make the uterine lining less receptive, so results are equal or better in most patients and clearly better in strong responders. Fresh transfer remains appropriate for many women with a normal response and a good lining.
Vitrified embryos do not deteriorate measurably over time in storage, and healthy babies have been born from embryos frozen for many years. The practical limit is set by national regulations and by the consent forms you sign with your clinic rather than by biology. Storage usually carries an annual fee, so ask for that figure in writing and check what happens if a payment is missed.
A freeze-all cycle means all embryos are frozen and none transferred in the stimulation cycle itself. It is recommended when a woman has responded strongly and is at risk of ovarian hyperstimulation, since pregnancy in that cycle would worsen it; when the uterine lining is not receptive; when progesterone rises too early during stimulation; when embryos are undergoing genetic testing; or when embryos are being accumulated across several cycles.
Modern vitrification achieves high survival rates through thawing, and large studies have not shown an increase in birth defects in babies born from frozen embryos compared with fresh. Babies from frozen transfers are on average slightly heavier at birth, with somewhat lower rates of low birth weight and preterm delivery. Medicated frozen cycles do carry a slightly higher rate of hypertensive disorders in pregnancy.
There is no ovarian stimulation, no egg collection and no sedation. The lining is prepared either by tracking your natural ovulation or with oestrogen tablets or patches, monitored by ultrasound over about two weeks. Progesterone is then started, which sets the transfer date. On the day, the embryo is thawed and its survival confirmed, then placed into the uterus through a fine catheter under ultrasound guidance in a few minutes without anaesthesia.
No. Studies consistently show no benefit from bed rest after embryo transfer, and prolonged lying down may be marginally counterproductive. Return to normal light activity, avoid heavy lifting and very strenuous exercise, and take your progesterone exactly as prescribed. The embryo will not be dislodged by standing, walking or ordinary daily movement.