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    Fresh vs. Frozen Embryo Transfer: Is Vitrify All a Better Option? A Retrospective Study

    Fresh vs. Frozen Embryo Transfer: Is Vitrify All a Better Option? A Retrospective Study

    Rosli NI, Hing KK, Tham MY, Sim PK, Lim YH, Nadkarni P. Is Vitrify All a Better Option? Poster presented at the ASPIRE (Asia Pacific Initiative on Reproduction) Conference, 2014. KL Fertility Centre, Kuala Lumpur, Malaysia.

    Presented: 2014 | Last reviewed: July 2026

    This page summarises findings from a conference poster presentation based on clinical data from KL Fertility & Gynaecology Centre. It is presented here for the clinical and scientific community and is not intended as a substitute for individualised patient counselling.

    Funding and disclosures: No declarations available (conference poster). The authors report no competing interests.

    Background and Rationale

    Frozen embryo transfer (FET) has been reported to carry a lower risk of prenatal bleeding, preterm delivery, and low birth weight compared with fresh embryo transfer. Implantation rate may also be improved in a non-stimulated cycle, as controlled ovarian hyperstimulation (COH) can adversely affect embryo-endometrium synchrony. These observations prompted interest in a “freeze-all” strategy: vitrifying all available embryos following egg collection and deferring all transfers to subsequent FET cycles.

    The key clinical question this study sought to address was whether, in the same group of patients who experienced both a fresh transfer and a subsequent frozen transfer, the frozen cycle produced meaningfully better outcomes — and if so, whether a policy of vitrifying all embryos might improve cumulative clinical pregnancy rates.

    Study Design and Methods: NC, m-NC, and HRT Protocols for FET

    Design: 

    Retrospective study.

    Subjects:

    190 patients below age 42 who had fresh embryo transfer at KL Fertility Centre in 2012 and had surplus embryos vitrified. Of these, 107 subsequently underwent frozen embryo transfer using the vitrified surplus embryos.

    Pre-transfer screening:

    Prior to each transfer (fresh and frozen), elevated progesterone on the day of trigger, risk of OHSS, presence of polyps, and other factors were evaluated.

    Comparison: 

    Fresh ET outcomes (n=190) versus Frozen ET outcomes (n=107) within the same original patient group. Outcomes tracked through end of first trimester (approximately 12 weeks’ gestation).

    Outcome measures: 

    Biochemical pregnancy rate (positive hCG per ET), clinical pregnancy rate (intrauterine sac per ET, continued through first trimester per poster definition), and miscarriage rate (miscarriages per biochemical pregnancy).

    Statistical analysis: 

    Chi-square (χ²) analysis. Significance threshold: p < 0.05.

    Results: Clinical Pregnancy and Miscarriage Rates

    Table 1. Fresh ET vs. Frozen ET outcomes

    Outcome

    Fresh ET (n=190)

    Frozen ET (n=107)

    Biochemical pregnancy rate

     51.05%

    57.01%

    Clinical pregnancy rate

    36.84%

    50.47%

    Miscarriage rate

    27.84%

    11.48%

    Using chi-square analysis, clinical pregnancy rate was significantly higher (p < 0.05) and miscarriage rate was significantly lower (p < 0.05) in the frozen embryo transfer group compared with the fresh transfer group.

    Discussion: How These Findings Compare With Published Evidence

    The significantly higher clinical pregnancy rate and lower miscarriage rate in the FET group are consistent with the hypothesis that COH impairs embryo-endometrium synchrony during a fresh cycle, and that transfer in a subsequent non-stimulated cycle benefits from a more receptive uterine environment.

    These findings are broadly consistent with the wider literature. Meta-analyses of randomised controlled trials have found significantly higher live birth and clinical pregnancy rates, and lower miscarriage and OHSS rates, in freeze-all strategies compared with fresh transfer. However, evidence also indicates that the magnitude of benefit is not uniform: the freeze-all advantage is most pronounced in high responders and in women with polycystic ovary syndrome (PCOS), and less clear in women with a typical ovarian response. A 2021 Cochrane review found that for non-PCOS women with a normal ovarian response, freeze-all did not clearly improve live birth rates over fresh transfer, while it did reliably reduce OHSS risk. Current ESHRE guidance reserves elective freeze-all as standard practice specifically for high-risk or high-response groups rather than recommending it universally.

    As a 2014 conference poster based on 2012 data, this study predates the more nuanced current view. Its conclusion that there is “a role to vitrify all embryos” reflects the state of evidence at the time and the clear benefit seen in this centre’s early cohort data, but should be contextualised within the subsequent literature as a group-specific rather than universal recommendation.

    Clinical Practice Implications

    These data support the use of frozen embryo transfer for patients with vitrified surplus embryos, consistent with current practice. For clinicians weighing a freeze-all strategy at the outset of an IVF cycle, the key patient-level factors to consider are ovarian response profile, PCOS status, and OHSS risk, since these are the populations where current evidence most robustly supports elective freeze-all. For typical responders without these risk factors, fresh transfer remains a clinically supported option.

    Limitations of This Retrospective Study

    • Study design: retrospective, non-randomised, within-patient comparison. The 107 patients who underwent FET represent a subset of the original 190; this subset is not necessarily representative of all 190 (e.g. they may disproportionately represent women whose fresh cycle did not result in pregnancy, or those with higher-quality surplus embryos).
    • The poster reports only an overall p < 0.05 threshold without individual p-values, confidence intervals, or effect size estimates for each outcome.
    • Data were collected in 2012 and presented in 2014, predating vitrification technique refinements and the more nuanced evidence base that has since developed.
    • No data on endometrial preparation protocol, embryo stage, or embryo quality for the FET group are provided.
    • Short-term follow-up only (through first trimester); no live birth data reported.
    • The sample size discrepancy (n=170 as printed vs. n=107 as calculated from stated percentages) in the Frozen ET group is documented above; confirmed n=107 is used throughout this summary.
    • Conference poster format; not peer-reviewed in a journal.

    Key Findings

    • In a retrospective comparison within the same patient group, frozen embryo transfer produced a significantly higher clinical pregnancy rate than fresh embryo transfer (50.47% vs. 36.84%; p < 0.05).
    • Miscarriage rate was significantly lower following frozen embryo transfer than fresh transfer (11.48% vs. 27.84%; p < 0.05).
    • These findings support frozen embryo transfer as a preferred strategy for patients with vitrified surplus embryos, consistent with the broader literature.
    • Current evidence supports elective freeze-all most strongly for high responders and PCOS patients; the benefit in typical responders is less clearly established.

    About the Team Behind This Research

    • Nur Ilanah Rosli, Hing Kah Kei and Poo-Keen Sim were members of the clinical and scientific team at KL Fertility & Gynaecology Centre.
    • Jasmine Tham Mei Yeong is a Senior Embryologist at KL Fertility & Gynaecology Centre, with over 10 years of experience. (Profile: MSART — Malaysian Society of Assisted Reproductive Technology)
    • Dr. Yun-Hsuen (Helena) Lim is a Fertility Specialist and Consultant in Obstetrics & Gynaecology at KL Fertility & Gynaecology Centre. Fellow of the Royal College of Obstetricians and Gynaecologists (UK); Master’s degree from Universiti Kebangsaan Malaysia.
    • Dato' Dr. Prashant Nadkarni is a Fertility Specialist in Reproductive Medicine at KL Fertility & Gynaecology Centre.

    References

    1. Zhang W, Xiao X, Zhang J, Wang W, Wu J, Peng L, Wang X. Clinical outcomes of frozen embryo versus fresh embryo transfer following in vitro fertilization: a meta-analysis of randomized controlled trials. Archives of Gynecology and Obstetrics, 2018;298(2):259-272.
    2. Dieamant FC, Petersen CG, Mauri AL, Comar V, Mattila M, Vagnini LD, Renzi A, Petersen B, Nicoletti A, Oliveira JBA, Baruffi RL, Franco JG Jr. Fresh embryos versus freeze-all embryos: transfer strategies, nuances of a meta-analysis. JBRA Assisted Reproduction, 2017;21(3):260-272.
    3. Zaat T, Zagers M, Mol F, Goddijn M, van Wely M, Mastenbroek S. Fresh versus frozen embryo transfers in assisted reproduction. Cochrane Database of Systematic Reviews, 2021;2:CD011184.
    4. ESHRE Add-ons working group, Lundin K, Bentzen JG, Bozdag G, et al. Good practice recommendations on add-ons in reproductive medicine. Human Reproduction, 2023;38(11):2062-2104.