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Completed

NCT Number: NCT03765359

Metformin Use to Improve Pregnancy Outcome in Women With Type 1 Diabetes.

The study investigates whether additional metformin medication in combination with regular insulin treatment will decrease the need of insulin for women with diabetes mellitus type 1 during pregnancy.

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Key information

Sex eligibility

Female

Study type

Interventional

Phase

Phase 4

Primary location

Helsinki University Hospital, Helsinki, Finland

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About this study

Insulin resistance during pregnancy of diabetes mellitus type 1 patients (DM1) increases the need for insulin and makes it more difficult to maintain normoglycemia. Fetal exposure to hyperglycemia induces macrosomia which increases fetal and neonatal morbidity and mortality. Further more obesity and excess weight gain during pregnancy enhances insulin resistance and it's an independent risk factor for fetal macrosomia.

Metformin is a medical treatment for type 2 diabetes (DM2) where consequential pathophysiology includes insulin resistance. It reduces hepatic glucose production and enhances the use of glucose in muscles relieving insulin resistance. Metformin has also found to inhibit weight gain effectively.

Metformin has approved to be safe and effective in patients with gestational diabetes (GDM). It has found to reduce weight gain and improve postprandial blood glucose levels during pregnancy and reduce neonatal birth trauma in GDM. However, there are no previous studies about the use of metformin in pregnant women with DM1.

Two hundred women with DM1 will be randomized to get placebo or metformin in addition to regular insulin treatment. The sample size has been estimated to demonstrate the difference of 15 % in the need to increase insulin dosages during the pregnancy between the study groups.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • a pregnancy of a woman with type 1 diabetes.

Exclusion criteria

  • multiple pregnancy, significant underlying disease (hearth disease, kidney transplant, IBD (inflammatory bowel disease ), SLE (systemic lupus erythematosus ), diseases with use of high dosage corticosteroids (severe asthma or rheumatic disease), severe complications of diabetes (nephropathy, neuropathy, gastroparesis or severe retinopathy), substance abuse, smoking, BMI <18, strong early pregnancy nausea (=hyperemesis)

Treatment and study plan

metforminhydrochloride

Drug

metformin 500 mg tablets and insulin

Other names: A10BA02, Diformin, Metformin

Placebo oral tablet

Drug

Placebo tablets mimic metformin 500 mg tablets and insulin

Primary outcomes

  1. Changes in the insulin need during pregnancy

    Time frame: from 5-10 gestational weeks until the delivery

    The insulin dosage (IU/ml) in two weeks sets

Secondary outcomes

  1. Blood glucose balance during pregnancy HbA1c

    Time frame: from gestational weeks 5 until the delivery

    HbA1c (mmol/mol)

  2. Blood glucose balance during pregnancy AVG, SD, CV

    Time frame: from gestational weeks 5 until the delivery

    mean blood glucose (mmol/l) level, standard deviation (SD) and the coefficient of variation of the blood glucose levels

  3. Change in the weight

    Time frame: from gestational weeks 5 until the delivery

    Weight gain (g) during pregnancy

  4. Change in the blood pressure

    Time frame: from gestational weeks 5 until the delivery

    Blood pressure (mmHg)

  5. Incidence of pre-eclampsia

    Time frame: from gestational weeks 20 until the delivery

    Incidence of pre-eclampsia (%)

  6. Incidence hepatogestosis

    Time frame: from gestational weeks 20 until the delivery

    Incidence hepatogestosis (%)

  7. Pregnancy complications

    Time frame: from gestational weeks 5 until the delivery

    Incidence proteinuria (mg/mmol or mg/d)

  8. macrosomia

    Time frame: from gestational weeks 20 until the delivery

    estimated fetal weight in ultrasound (grams)

  9. Pregnancy complications

    Time frame: 12-22 weeks of gestation

    incidence of miscarriage (intrauterine death before 22 weeks of gestation or fetal weigth under 500g) (%)

  10. Pregnancy complications

    Time frame: 22-40 weeks of gestation

    incidence of intrauterine death (intrauterine death after 22 weeks of gestation or fetal weigth over 500g) (%)

  11. Thigh fractional volume ultrasound

    Time frame: from gestational weeks 20 until delivery

    Fetal weight estimation (g) is specified by thigh fractional volume ultrasound program

  12. Rate of the caesarean sections

    Time frame: The delivery

    Rate of the caesarean sections (%)

  13. Labour

    Time frame: The delivery

    rate of spontaneous delivery (%)

  14. Rate of the operative vaginal deliveries

    Time frame: The delivery

    Rate of the operative vaginal deliveries (%)

  15. Rate of the shoulder dystocia

    Time frame: The delivery

    Rate of the shoulder dystocia (%)

  16. Labor complications

    Time frame: The delivery

    rate of induced delivery (%)

  17. Rate of the perineal tears

    Time frame: The delivery

    Rate of the perineal tears (%)

  18. Postpartum bleeding

    Time frame: The delivery

    postpartum bleeding (ml)

  19. Newborn variables (gestational age)

    Time frame: After the delivery

    Rate of the premature deliveries (=deliveries before 37 weeks of gestation) (%)

  20. Newborn variables

    Time frame: After the delivery

    weight of the newborn (g)

  21. Newborn outcome

    Time frame: After the delivery

    Acidosis of the newborn (pH)

  22. Newborn outcome (intensive care)

    Time frame: After the delivery

    The need of NICU (neonatal intensive care unit) treatment (days)

  23. Newborn outcome (hypoglycemia)

    Time frame: After the delivery

    The occurrence of hypoglycemia (=plasma glucose under 2.6mmol/l or usage of iv glucose infusion) (%)

  24. Newborn outcome (Erb's)

    Time frame: After the delivery

    Incidence of the Erb's paresis (%)

  25. Cost benefit calculations (sick leaves)

    Time frame: from gestational weeks 12 until delivery

    The need of sick leaves during pregnancy (days)

  26. Cost benefit calculations (visits to maternity outpatient clinic or internal medicine policlinic)

    Time frame: 14-40 weeks of gestation

    The need of polyclinical controls during pregnancy (number of visits/pregnancy)

  27. Cost benefit calculations (hospitalization)

    Time frame: 14-40 weeks of gestation

    The need of hospitalization during pregnancy (days/pregnancy)

  28. Cost benefit calculations (all outpatient visits after delivery )

    Time frame: One year after the delivery

    The need of policlinical controls of the diabetic mother after the delivery (number of visits)

  29. Cost benefit calculations (hospitalization after delivery, all departments)

    Time frame: Up to one year after the delivery

    The need of hospitalization of the diabetic mother after the delivery (days)

  30. Cost benefit calculations (all hospitalization of the child)

    Time frame: Until the age of one year

    The need of hospitalization of the child (days)

  31. Cost benefit calculations (all policlinical controls of the child)

    Time frame: Until the age of one year

    The need of policlinical controls of the child (number of visits)

  32. high sensitive-CRP

    Time frame: 7-10, 26-28 and 34-36 weeks of gestation

    high sensitive-CRP (mg/l)

  33. lipids

    Time frame: 7-10, 26-28 and 34-36 weeks of gestation

    cholesterol, high density lipoprotein, low density lipoprotein, triglyserids (mmol/l)

  34. Inflammatory markers

    Time frame: 7-10, 26-28 and 34-36 weeks of gestation

    adiponectin, leptin, resistin, IL-6, TNF-α (pg/ml)

Sponsors and collaborators

Lead sponsor

Tampere University Hospital

Other

Collaborators

  • Central Finland Hospital District
  • Helsinki University Central Hospital
  • Oulu University Hospital
  • Turku University Hospital

Registry information

Official study title

Metformin Use to Improve Pregnancy Outcome in Women With Type 1 Diabetes. A Randomized Double-blind Placebo-controlled Multicenter Study.

Important dates

Study start
2019
Primary completion
2022
Study completion
2022
First posted
Dec 5, 2018
Registry last updated
Jun 7, 2023

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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