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NCT Number: NCT06064669

Effect of Metformin on Healthy Live Birth in Women With Prediabetes

To evaluate the efficacy and safety of metformin pretreatment on reproductive outcomes in infertile women with prediabetes.

Recruiting

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Key information

Age range

20 year–40 year

Sex eligibility

Female

Study type

Interventional

Phase

Not applicable

Primary location

About this study

To evaluate the efficacy and safety of metformin pretreatment on reproductive outcomes in infertile women with prediabetes and to determine whether either starting metformin pretreatment before ovarian stimulation (aiming at improving the quality of oocyte/embryo) or starting before frozen embryo transfer (FET) (aiming at improving the receptivity of endometrium) could increase the chance of a healthy live birth compared with placebo.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Women who are diagnosed with prediabetes by ADA criteria, including either IFG, IGT, or HbA1C 5.7-6.4%.
  • Women aged 20-40 years.
  • Women who plan to undergo a new cycle of IVF, ICSI, or PGT-A.

Exclusion criteria

  • Women who are diagnosed with diabetes according to the ADA criteria11,12, which is meeting one of the following criteria: fasting plasma glucose ≥7.0mmol/L, 2-h plasma glucose during 75-g OGTT ≥11.1mmol/L, HbA1c≥6.5%, or a random plasma glucose≥11.1mmol/L.
  • Women who are taking medicine that interfere with glucose metabolism, such as metformin, oral anti-diabetic agents (sulfonylureas, glinides, thiazolidinediones, α-glycosidase inhibitors, GLP-1 receptor agonist, etc.), weight loss drugs (i.e.orlistat, etc.), glucocorticoids, and growth hormones within 2 months before enrollment.
  • Women with un-corrected hyperthyroidism or hypothyroidism.
  • Women with congenital or acquired abnormal uterine cavity including septate uterus, unicornous uterus, uterus duplex, and intrauterine adhesions.
  • Women with a diagnosis of adenomyosis.
  • Women with untreated hydrosalpinx.
  • Women who plan to undergo PGT-SR or PGT-M.
  • Women with major medical comorbidities, such as known liver disease, known renal disease, or known significant anemia.

Treatment and study plan

Metformin pretreatment before ovarian stimulation

Drug

The enrolled patients will be prescribed metformin 850mg twice daily for at least 4 weeks prior to ovarian stimulation till oocyte retrieval.

Other names: Metformin before ovarian stimulation

Placebo pretreatment before ovarian stimulation

Drug

The enrolled patients will be prescribed placebo 850mg twice daily for at least 4 weeks prior to ovarian stimulation till oocyte retrieval.

Other names: Placebo before ovarian stimulation

Metformin pretreatment before endometrial preparation for frozen embryo transfer

Drug

After oocyte retrieval, the enrolled patients will be prescribed metformin 850mg twice daily for at least 4 weeks before endometrial preparation for frozen embryo transfer and till the establishment of clinical pregnancy (7-8 weeks gestation) after the first frozen embryo transfer.

Other names: Metformin before endometrial preparation

Placebo pretreatment before endometrial preparation for frozen embryo transfer

Drug

After oocyte retrieval, the enrolled patients will be prescribed placebo 850mg twice daily for at least 4 weeks before endometrial preparation for frozen embryo transfer and till the establishment of clinical pregnancy (7-8 weeks gestation) after the first frozen embryo transfer.

Other names: Placebo before endometrial preparation

Primary outcomes

  1. healthy live birth

    Time frame: From the date of randomization until delivery after the first embryo transfer, up to 16 months

    defined as a singleton live birth at ≥37 weeks, with infant birth weight between 2500 and 4000g and without a major congenital anomaly.

Secondary outcomes

  1. Change in BMI

    Time frame: From the date of randomization until the establishment of clinical pregnancy after the first embryo transfer, up to 26 weeks

    change in body mass index (BMI) from baseline to the establishment of clinical pregnancy.

  2. Change in fasting glucose level

    Time frame: From the date of randomization until the establishment of clinical pregnancy after the first embryo transfer, up to 26 weeks

    change in fasting glucose level from baseline to the establishment of clinical pregnancy.

  3. Change in fasting insulin level

    Time frame: From the date of randomization until the establishment of clinical pregnancy after the first embryo transfer, up to 26 weeks

    change in fasting insulin level from baseline to the establishment of clinical pregnancy.

  4. Change in 2-h levels of glucose after 75-g OGTT

    Time frame: From the date of randomization until the establishment of clinical pregnancy after the first embryo transfer, up to 26 weeks

    change in 2-h levels of glucose after 75-g OGTT from baseline to the establishment of clinical pregnancy.

  5. Change in 2-h levels of insulin after 75-g OGTT

    Time frame: From the date of randomization until the establishment of clinical pregnancy after the first embryo transfer, up to 26 weeks

    change in 2-h levels of insulin after 75-g OGTT from baseline to the establishment of clinical pregnancy.

  6. Days of ovarian stimulation

    Time frame: From the date of randomization until the day of oocyte retrieved, up to 12 weeks

    the duration of ovarian stimulation by exogenous gonadotropin

  7. Total dose of gonadotropins

    Time frame: From the date of randomization until the day of oocyte retrieved, up to 12 weeks

    the total dose of exogenous gonadotropin used during ovarian stimulation

  8. Peak estradiol level

    Time frame: From the date of randomization until the day of oocyte retrieved, up to 12 weeks

    the estradiol level on the day of hCG trigger

  9. Number of oocyte retrieved

    Time frame: From the date of randomization until the day of oocyte retrieved, up to 12 weeks

    the number of oocyte retrieved

  10. Number of good-score embryos

    Time frame: From the date of randomization until the third day after oocyte retrieval, up to 12 weeks

    the number of good-score embryos

  11. Number of euploid embryos

    Time frame: From the date of randomization until the initiation of endometrial preparation for frozen embryo transfer, up to 20 weeks

    the number of euploid embryos

  12. OHSS

    Time frame: From the day of oocyte retrieved until the initiation of endometrial preparation for the first frozen embryo transfer, up to 8 weeks

    ovarian hyperstimulation syndrome was defined according to the Golan criteria

  13. Clinical pregnancy

    Time frame: 30-35 days after the first frozen embryo transfer

    defined as the ultrasound confirmation of at least one intrauterine gestational sac

  14. Singleton or twin pregnancy

    Time frame: 30-35 days after the first frozen embryo transfer

    the number of intrauterine gestational sacs

  15. Pregnancy loss

    Time frame: From the date of confirmation of pregnancy until the date of pregnancy loss, up to 9 months

    defined as pregnancies that eventuate in a spontaneous abortion or therapeutic abortion that occurred throughout pregnancy.

  16. Live birth

    Time frame: From the date of randomization until delivery after the first embryo transfer, up to 16 months

    defined as the delivery of any neonate with signs of life at ≥ 28 weeks of gestation

  17. Incidences of obstetric and neonatal complications

    Time frame: From the establishment of clinically recognized pregnancy until six weeks after delivery after the first embryo transfer, up to 11 months

    including gestational diabetes mellitus, pre-eclampsia, premature rupture of membrane, placenta previa, placental abruption, congenital anomalies, postpartum hemorrhage, stillbirth, neonatal respiratory distress syndrome, neonatal jaundice, neonatal infection, neonatal death.

  18. Gestational weight gain

    Time frame: at delivery

    maternal weight gain during pregnancy

  19. Birth weight

    Time frame: at delivery

    birth weight of the newborn at delivery

  20. LGA

    Time frame: at delivery

    defined as the birthweight above the 90th percentile for gestational age based on a sex-specific reference

  21. SGA

    Time frame: at delivery

    defined as the birthweight below the 10th percentile for gestational age based on a sex-specific reference

  22. LBW

    Time frame: at delivery

    the infant born weighing less than 2500g

  23. Macrosomia

    Time frame: at delivery

    the infant born weighing larger than 4000g

  24. Adverse events

    Time frame: From the date of randomization until six weeks after delivery after the first embryo transfer, up to 18 months

    adverse event (AE) and serious adverse event (SAE)

  25. Cumulative live birth

    Time frame: From the date of randomization until delivery, up to 28 months

    define as women achieving live birth after all the cycles of embryo transfer per oocyte retrieval that performed within one year after randomization.

Study contacts

Contact information is provided by the study sponsor or research team.

Zi-Jiang Chen, Professor

CONTACT

[email protected]

+0086 531 85651190

Sponsors and collaborators

Lead sponsor

Shandong University

Other

Collaborators

  • General Hospital of Ningxia Medical University
  • Henan Provincial Maternal and Child Health Care Hospital
  • Nanjing Medical University
  • Qingdao women's and children's Hospital
  • Ren Ji Hospital of Shanghai Jiao Tong University
  • Shengjing Hospital
  • West China Second University Hospital
  • Women's Hospital of Zhejiang University

Registry information

Official study title

Effect of Metformin on Healthy Live Birth After In-vitro Fertilization in Women With Prediabetes Mellitus: a Multicenter Double-blind Placebo Controlled Randomized Trial

Acronym: MELT-PreDM

Important dates

Study start
2024
Primary completion
2026
Study completion
2027
First posted
Oct 3, 2023
Registry last updated
May 29, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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