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

Primary Purpose

Diabetic Pregnancy, Insulin Resistance, Type1diabetes

Status
Completed
Phase
Phase 4
Locations
Finland
Study Type
Interventional
Intervention
metforminhydrochloride
Placebo Oral Tablet
Sponsored by
Tampere University Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Diabetic Pregnancy focused on measuring insulin need, diabetic pregnancy, insulin resistance, metformin

Eligibility Criteria

undefined - undefined (Child, Adult, Older Adult)FemaleDoes not accept healthy volunteers

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)

Sites / Locations

  • Helsinki University Hospital
  • Central Finland Health Care District
  • Oulu University hospital
  • Tampere University Hospital
  • Turku University Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Placebo Comparator

Arm Label

metforminhydrochloride

Placebo Oral Tablet

Arm Description

Metformin medication starts on 12-14 weeks of gestation. The starting dosage is 1 tablet (500 mg) x1 and it is increased gradually 1 tablet a week up to 2+2 tablets (2000mg) daily. Duration of the treatment is approximately until one week before delivery. Otherwise metformin treatment combined with regular insulin and follow-up during pregnancy follows the national guidelines.

Placebo tablets starts on 12-14 weeks of gestation. The starting dosage is 1 tablet x1 and it is increased gradually 1 tablet a week up to 2+2 tablets daily. Duration of the treatment is approximately until one week before delivery. Otherwise placebo treatment combined with regular insulin and follow-up during pregnancy follows the national guidelines.

Outcomes

Primary Outcome Measures

Changes in the insulin need during pregnancy
The insulin dosage (IU/ml) in two weeks sets

Secondary Outcome Measures

Blood glucose balance during pregnancy HbA1c
HbA1c (mmol/mol)
Blood glucose balance during pregnancy AVG, SD, CV
mean blood glucose (mmol/l) level, standard deviation (SD) and the coefficient of variation of the blood glucose levels
Change in the weight
Weight gain (g) during pregnancy
Change in the blood pressure
Blood pressure (mmHg)
Incidence of pre-eclampsia
Incidence of pre-eclampsia (%)
Incidence hepatogestosis
Incidence hepatogestosis (%)
Pregnancy complications
Incidence proteinuria (mg/mmol or mg/d)
macrosomia
estimated fetal weight in ultrasound (grams)
Pregnancy complications
incidence of miscarriage (intrauterine death before 22 weeks of gestation or fetal weigth under 500g) (%)
Pregnancy complications
incidence of intrauterine death (intrauterine death after 22 weeks of gestation or fetal weigth over 500g) (%)
Thigh fractional volume ultrasound
Fetal weight estimation (g) is specified by thigh fractional volume ultrasound program
Rate of the caesarean sections
Rate of the caesarean sections (%)
Labour
rate of spontaneous delivery (%)
Rate of the operative vaginal deliveries
Rate of the operative vaginal deliveries (%)
Rate of the shoulder dystocia
Rate of the shoulder dystocia (%)
Labor complications
rate of induced delivery (%)
Rate of the perineal tears
Rate of the perineal tears (%)
Postpartum bleeding
postpartum bleeding (ml)
Newborn variables (gestational age)
Rate of the premature deliveries (=deliveries before 37 weeks of gestation) (%)
Newborn variables
weight of the newborn (g)
Newborn outcome
Acidosis of the newborn (pH)
Newborn outcome (intensive care)
The need of NICU (neonatal intensive care unit) treatment (days)
Newborn outcome (hypoglycemia)
The occurrence of hypoglycemia (=plasma glucose under 2.6mmol/l or usage of iv glucose infusion) (%)
Newborn outcome (Erb's)
Incidence of the Erb's paresis (%)
Cost benefit calculations (sick leaves)
The need of sick leaves during pregnancy (days)
Cost benefit calculations (visits to maternity outpatient clinic or internal medicine policlinic)
The need of polyclinical controls during pregnancy (number of visits/pregnancy)
Cost benefit calculations (hospitalization)
The need of hospitalization during pregnancy (days/pregnancy)
Cost benefit calculations (all outpatient visits after delivery )
The need of policlinical controls of the diabetic mother after the delivery (number of visits)
Cost benefit calculations (hospitalization after delivery, all departments)
The need of hospitalization of the diabetic mother after the delivery (days)
Cost benefit calculations (all hospitalization of the child)
The need of hospitalization of the child (days)
Cost benefit calculations (all policlinical controls of the child)
The need of policlinical controls of the child (number of visits)
high sensitive-CRP
high sensitive-CRP (mg/l)
lipids
cholesterol, high density lipoprotein, low density lipoprotein, triglyserids (mmol/l)
Inflammatory markers
adiponectin, leptin, resistin, IL-6, TNF-α (pg/ml)

Full Information

First Posted
April 24, 2018
Last Updated
June 6, 2023
Sponsor
Tampere University Hospital
Collaborators
Turku University Hospital, Oulu University Hospital, Helsinki University Central Hospital, Central Finland Hospital District
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1. Study Identification

Unique Protocol Identification Number
NCT03765359
Brief Title
Metformin Use to Improve Pregnancy Outcome in Women With Type 1 Diabetes.
Official Title
Metformin Use to Improve Pregnancy Outcome in Women With Type 1 Diabetes. A Randomized Double-blind Placebo-controlled Multicenter Study.
Study Type
Interventional

2. Study Status

Record Verification Date
June 2023
Overall Recruitment Status
Completed
Study Start Date
August 5, 2019 (Actual)
Primary Completion Date
December 19, 2022 (Actual)
Study Completion Date
December 19, 2022 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Tampere University Hospital
Collaborators
Turku University Hospital, Oulu University Hospital, Helsinki University Central Hospital, Central Finland Hospital District

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No

5. Study Description

Brief Summary
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.
Detailed Description
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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Diabetic Pregnancy, Insulin Resistance, Type1diabetes
Keywords
insulin need, diabetic pregnancy, insulin resistance, metformin

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigator
Masking Description
placebo controlled
Allocation
Randomized
Enrollment
101 (Actual)

8. Arms, Groups, and Interventions

Arm Title
metforminhydrochloride
Arm Type
Active Comparator
Arm Description
Metformin medication starts on 12-14 weeks of gestation. The starting dosage is 1 tablet (500 mg) x1 and it is increased gradually 1 tablet a week up to 2+2 tablets (2000mg) daily. Duration of the treatment is approximately until one week before delivery. Otherwise metformin treatment combined with regular insulin and follow-up during pregnancy follows the national guidelines.
Arm Title
Placebo Oral Tablet
Arm Type
Placebo Comparator
Arm Description
Placebo tablets starts on 12-14 weeks of gestation. The starting dosage is 1 tablet x1 and it is increased gradually 1 tablet a week up to 2+2 tablets daily. Duration of the treatment is approximately until one week before delivery. Otherwise placebo treatment combined with regular insulin and follow-up during pregnancy follows the national guidelines.
Intervention Type
Drug
Intervention Name(s)
metforminhydrochloride
Other Intervention Name(s)
A10BA02, Diformin, Metformin
Intervention Description
metformin 500 mg tablets and insulin
Intervention Type
Drug
Intervention Name(s)
Placebo Oral Tablet
Intervention Description
Placebo tablets mimic metformin 500 mg tablets and insulin
Primary Outcome Measure Information:
Title
Changes in the insulin need during pregnancy
Description
The insulin dosage (IU/ml) in two weeks sets
Time Frame
from 5-10 gestational weeks until the delivery
Secondary Outcome Measure Information:
Title
Blood glucose balance during pregnancy HbA1c
Description
HbA1c (mmol/mol)
Time Frame
from gestational weeks 5 until the delivery
Title
Blood glucose balance during pregnancy AVG, SD, CV
Description
mean blood glucose (mmol/l) level, standard deviation (SD) and the coefficient of variation of the blood glucose levels
Time Frame
from gestational weeks 5 until the delivery
Title
Change in the weight
Description
Weight gain (g) during pregnancy
Time Frame
from gestational weeks 5 until the delivery
Title
Change in the blood pressure
Description
Blood pressure (mmHg)
Time Frame
from gestational weeks 5 until the delivery
Title
Incidence of pre-eclampsia
Description
Incidence of pre-eclampsia (%)
Time Frame
from gestational weeks 20 until the delivery
Title
Incidence hepatogestosis
Description
Incidence hepatogestosis (%)
Time Frame
from gestational weeks 20 until the delivery
Title
Pregnancy complications
Description
Incidence proteinuria (mg/mmol or mg/d)
Time Frame
from gestational weeks 5 until the delivery
Title
macrosomia
Description
estimated fetal weight in ultrasound (grams)
Time Frame
from gestational weeks 20 until the delivery
Title
Pregnancy complications
Description
incidence of miscarriage (intrauterine death before 22 weeks of gestation or fetal weigth under 500g) (%)
Time Frame
12-22 weeks of gestation
Title
Pregnancy complications
Description
incidence of intrauterine death (intrauterine death after 22 weeks of gestation or fetal weigth over 500g) (%)
Time Frame
22-40 weeks of gestation
Title
Thigh fractional volume ultrasound
Description
Fetal weight estimation (g) is specified by thigh fractional volume ultrasound program
Time Frame
from gestational weeks 20 until delivery
Title
Rate of the caesarean sections
Description
Rate of the caesarean sections (%)
Time Frame
The delivery
Title
Labour
Description
rate of spontaneous delivery (%)
Time Frame
The delivery
Title
Rate of the operative vaginal deliveries
Description
Rate of the operative vaginal deliveries (%)
Time Frame
The delivery
Title
Rate of the shoulder dystocia
Description
Rate of the shoulder dystocia (%)
Time Frame
The delivery
Title
Labor complications
Description
rate of induced delivery (%)
Time Frame
The delivery
Title
Rate of the perineal tears
Description
Rate of the perineal tears (%)
Time Frame
The delivery
Title
Postpartum bleeding
Description
postpartum bleeding (ml)
Time Frame
The delivery
Title
Newborn variables (gestational age)
Description
Rate of the premature deliveries (=deliveries before 37 weeks of gestation) (%)
Time Frame
After the delivery
Title
Newborn variables
Description
weight of the newborn (g)
Time Frame
After the delivery
Title
Newborn outcome
Description
Acidosis of the newborn (pH)
Time Frame
After the delivery
Title
Newborn outcome (intensive care)
Description
The need of NICU (neonatal intensive care unit) treatment (days)
Time Frame
After the delivery
Title
Newborn outcome (hypoglycemia)
Description
The occurrence of hypoglycemia (=plasma glucose under 2.6mmol/l or usage of iv glucose infusion) (%)
Time Frame
After the delivery
Title
Newborn outcome (Erb's)
Description
Incidence of the Erb's paresis (%)
Time Frame
After the delivery
Title
Cost benefit calculations (sick leaves)
Description
The need of sick leaves during pregnancy (days)
Time Frame
from gestational weeks 12 until delivery
Title
Cost benefit calculations (visits to maternity outpatient clinic or internal medicine policlinic)
Description
The need of polyclinical controls during pregnancy (number of visits/pregnancy)
Time Frame
14-40 weeks of gestation
Title
Cost benefit calculations (hospitalization)
Description
The need of hospitalization during pregnancy (days/pregnancy)
Time Frame
14-40 weeks of gestation
Title
Cost benefit calculations (all outpatient visits after delivery )
Description
The need of policlinical controls of the diabetic mother after the delivery (number of visits)
Time Frame
One year after the delivery
Title
Cost benefit calculations (hospitalization after delivery, all departments)
Description
The need of hospitalization of the diabetic mother after the delivery (days)
Time Frame
Up to one year after the delivery
Title
Cost benefit calculations (all hospitalization of the child)
Description
The need of hospitalization of the child (days)
Time Frame
Until the age of one year
Title
Cost benefit calculations (all policlinical controls of the child)
Description
The need of policlinical controls of the child (number of visits)
Time Frame
Until the age of one year
Title
high sensitive-CRP
Description
high sensitive-CRP (mg/l)
Time Frame
7-10, 26-28 and 34-36 weeks of gestation
Title
lipids
Description
cholesterol, high density lipoprotein, low density lipoprotein, triglyserids (mmol/l)
Time Frame
7-10, 26-28 and 34-36 weeks of gestation
Title
Inflammatory markers
Description
adiponectin, leptin, resistin, IL-6, TNF-α (pg/ml)
Time Frame
7-10, 26-28 and 34-36 weeks of gestation

10. Eligibility

Sex
Female
Gender Based
Yes
Gender Eligibility Description
Study is done during pregnancy
Accepts Healthy Volunteers
No
Eligibility Criteria
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)
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Kati Tihtonen, PhD
Organizational Affiliation
Tampere University Hospital, Tampere University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Helsinki University Hospital
City
Helsinki
Country
Finland
Facility Name
Central Finland Health Care District
City
Jyväskylä
Country
Finland
Facility Name
Oulu University hospital
City
Oulu
Country
Finland
Facility Name
Tampere University Hospital
City
Tampere
Country
Finland
Facility Name
Turku University Hospital
City
Turku
Country
Finland

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

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

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