Flash Glucose Monitoring in Gestational Diabetes Mellitus: Study Protocol for a Randomized Controlled Trial
- Conditions
- Gestational Diabetes Mellitus
- Interventions
- Device: Flash Glucose MonitoringDevice: Self-Monitoring of Blood Glucose
- Registration Number
- NCT04422821
- Lead Sponsor
- Medical University of Warsaw
- Brief Summary
Gestational diabetes mellitus (GDM) is glucose intolerance diagnosed for the first time in pregnancy. According to literature GDM affects 3-10% of pregnant women and is a risk factor for multiple maternal and fetal complications. During pregnancy GDM significantly increases the risk of fetal macrosomia, shoulder dystocia, birth trauma and Cesarean section. Furthermore, the long-term complications of GDM include increased risk of development of diabetes mellitus type 2 in the mother, as well as increased risk of obesity, diabetes and metabolic syndrome occurrence in their children. It has been well-documented that the risk of above-mentioned complications increases with the level of maternal hyperglycemia.
Proper glycemia control is one of the key elements in the effective treatment of GDM. Until recently, glucose monitoring was solely performed using glucose meters, which required multiple fingerpricks. Nowadays, due to the glycemia monitoring systems development, such as flash glucose monitoring (FGM), glucose levels may be measured less invasively through subcutaneous sensor application. As shown in one of the studies, FGM due to the ease of use, was 3 times more often applied as a method of glycemia control than SMBG. As a result, patients from FGM group had significantly better blood glucose control.
The main purpose of our study is to evaluate the impact of new method of glycemia control (FGM) on the efficacy of treatment of GDM. By analyzing results of this study, such as mean glycemia levels, number of women requiring insulin therapy and maternal-fetal perinatal outcomes the investigators will provide a scientific basis for more common use of FGM in the population of pregnant women affected by GDM.
- Detailed Description
This is a randomized controlled trial performed at the 1st Department of Obstetrics and Gynecology of Medical University of Warsaw. The study will recruit 100 women at 24-28 weeks of gestation . Women diagnosed with GDM, who will meet the inclusion criteria, will be individually randomized to Flash Glucose Monitoring (n=50) or Self-Monitoring of Blood Glucose (n=50) group.
The study group will obtain instruction for using Freestyle Libre app to measure and collect glycemia results using a mobile phone.
The control group will be informed about proper use of glucose meters.
All participants will be obliged to measure fasting and 1-h postprandial glucose concentrations in a daily manner, together with once per week midnight measurement.
All participants will obtain dietary recommendations for gestational diabetes mellitus and recommendations about daily physical activity in pregnancy.
In order to assess daily physical activity all participants will obtain a wristband allowing for footsteps measurement.
An evaluation of patient's dietary habits will be based on Eating Assessment Test prepared by the Polish National Institute of Public Health - National Institute of Hygiene.
Clinical and laboratory results of the mother and their newborns will be collected for analysis during the course of pregnancy.
After delivery, at the follow-up visit research staff will retrieve maternal and neonatal outcomes from patients medical history.
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- Female
- Target Recruitment
- 100
- age ≥ 18 years
- singleton pregnancy between 24-28 weeks of gestation
- gestational diabetes mellitus diagnosis
- multiple pregnancy
- fetal malformations
- pre-gestational diabetes mellitus
- chronic or pregnancy-induced hypertension
- chronic renal or hepatic disease, in-vitro fertilization
- delivery <37 weeks of gestation
- pre-mature rupture of membranes
- placenta previa
- stillbirth
- smoking in pregnancy
- intake of medications including: methyldopa, tetracyclin, acetylosalicylic acid, acetaminofen, ibuprofen, L-dopa, tolazamide, tolbutamide
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- CROSSOVER
- Arm && Interventions
Group Intervention Description FreeStyle Libre™ Flash Glucose Monitoring FreeStyle Libre™ will comprise 50 pregnant women between 24-28 weeks of gestation, diagnosed with gestational diabetes mellitus, who will receive subcutaneous sensor for glucose monitoring (FreeStyle Libre™; Abbott Diabetes Care, Alameda, CA) for 4 weeks. iXell® Self-Monitoring of Blood Glucose iXell® will comprise 50 pregnant women between 24-28 weeks of gestation, diagnosed with gestational diabetes mellitus, who will monitor glycemia through use of standard glucose meter (iXell®; Genexo sp; Warsaw, Poland) for 4 weeks.
- Primary Outcome Measures
Name Time Method Mean glycemia results (fasting and 1-h postprandial glucose concentrations) 28 days after the recruitment visit Glycemia results analysis according to Polish Society of Obstetricians and Gynecologists (PSOG) recommendations for gestational diabetes mellitus.
- Secondary Outcome Measures
Name Time Method Gestational weight gain 2, 4 and 8 weeks after the recruitment visit Gestational weight gain in each group will by analyzed at the second, third and fourth follow-up visit.
Physical activity during one month analysis 0-4 weeks after the recruitment visit Number of footsteps walk per day in each group will by analyzed at the third follow-up visit.
Number of patients requiring insulin therapy 2, 4 and 8 weeks after the recruitment visit Number of patients in each group requiring insulin therapy will by analyzed at the second, third and fourth follow-up visit.
Long-term glycemic control using blood HbA1c serum concentration 4 and 8 weeks after the recruitment visit Difference in HbA1c serum concentration in each group will by analyzed at the third and fourth follow-up visit.
Compliance with diet recommendations 2, 4 and 8 weeks after the recruitment visit Diet assessment in each group will be performed at the second, third and fourth follow-up visit to check compliance with diet recommendations.
Number of hypoglycemia episodes (glucose concentration <70 mg/dl) during one month analysis 0-4 weeks after the recruitment visit Number of hypoglycemia episodes in each group will by analyzed at third visit, to check whether there is a difference between the groups.
Mode of delivery (rate of vaginal delivery/ Cesarean section) 24-72 hours after the delivery Rate of vaginal delivery versus cesarean section in each group will by analyzed at the fifth follow-up visit.
Fetal birth-weight 24-72 hours after the delivery Fetal birth-weight in each group will by analyzed at the fifth follow-up visit.
Neonatal glycemia 24-72 hours after the delivery Neonatal glycemia in each group will by analyzed at the fifth follow-up visit, to check the rate of neonatal hypoglycemia.
Trial Locations
- Locations (1)
1st Department of Obstetrics and Gynecology, Medical University of Warsaw
🇵🇱Warsaw, Starynkiewicza Sq. 1/3, Poland