Shandong University
Jinan, Shandong, China
Location status: Recruiting
Location contact
Daimin Wei, Professor
CONTACT
Zi-Jiang Chen, Professor
CONTACT
NCT Number: NCT06064669
To evaluate the efficacy and safety of metformin pretreatment on reproductive outcomes in infertile women with prediabetes.
Interested in participating?
Request Info20 year–40 year
Female
Interventional
Not applicable
Jinan, Shandong, China
Location status: Recruiting
Daimin Wei, Professor
CONTACT
Zi-Jiang Chen, Professor
CONTACT
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.
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
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
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
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
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
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.
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.
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.
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.
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.
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.
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
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
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
Time frame: From the date of randomization until the day of oocyte retrieved, up to 12 weeks
the number of oocyte retrieved
Time frame: From the date of randomization until the third day after oocyte retrieval, up to 12 weeks
the number of good-score 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
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
Time frame: 30-35 days after the first frozen embryo transfer
defined as the ultrasound confirmation of at least one intrauterine gestational sac
Time frame: 30-35 days after the first frozen embryo transfer
the number of intrauterine gestational sacs
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.
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
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.
Time frame: at delivery
maternal weight gain during pregnancy
Time frame: at delivery
birth weight of the newborn at delivery
Time frame: at delivery
defined as the birthweight above the 90th percentile for gestational age based on a sex-specific reference
Time frame: at delivery
defined as the birthweight below the 10th percentile for gestational age based on a sex-specific reference
Time frame: at delivery
the infant born weighing less than 2500g
Time frame: at delivery
the infant born weighing larger than 4000g
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)
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.
Contact information is provided by the study sponsor or research team.
Shandong University
Other
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
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.
Published trials that share one or more normalized conditions with this study.
NCT07131384
Behavior, Diabetes Mellitus
Charlottesville, Virginia, United States
View Trial DetailsNCT06603480
Behavior, Diabetes Mellitus
Üsküdar, Istanbul, Turkey (Türkiye)
View Trial DetailsNCT02915198
Arterial Occlusive Diseases, Arteriosclerosis
Phoenix, Arizona, United States
View Trial DetailsNCT05532813
Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Genetic Diseases, Inborn
Garches, France
View Trial Details