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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04332393
Other study ID # 21-20POR
Secondary ID
Status Recruiting
Phase Phase 4
First received
Last updated
Start date May 15, 2020
Est. completion date December 2024

Study information

Verified date November 2023
Source The Baruch Padeh Medical Center, Poriya
Contact Enav Yefet, MD/PhD
Phone 972-46652306
Email enyefet@poria.health.gov.il
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Antenatal corticosteroids, particularly, betamethasone is routinely administered to pregnant women at risk for preterm delivery to improve neonatal outcomes. Although antenatal betamethasone was shown to induce both maternal hyperglycemia and neonatal hypoglycemia, to date, there is insufficient data to establish whether treatment for maternal hyperglycemia, particularly, metformin, will decrease the risk for neonatal hypoglycemia, particularly of preterm neonates. In the present study the investigators will examine the effect of treatment with metformin on maternal glycemic control and hypoglycemia in preterm neonates following maternal betamethasone treatment.


Recruitment information / eligibility

Status Recruiting
Enrollment 323
Est. completion date December 2024
Est. primary completion date April 2024
Accepts healthy volunteers No
Gender Female
Age group 18 Years and older
Eligibility Inclusion Criteria: - Pregnant women receiving betamethasone from 24 to 36.5 gestational weeks - Before or within 24 hours following the first dose of betamethasone - =18 years old Exclusion Criteria: - Women with pre-gestational and gestational diabetes mellitus (GDM) - Known allergic sensitivity to metformin - Known chronic heart failure - Known chronic renal failure - Refuse to participate - Refuse to perform glucose challenge test/glucose tolerance test later on

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Metformin
Metformin tablets according to glycemic control. Initial dose: 425 mg before meals (breakfast, lunch and supper) and 1700 mg around 22:00. Modifications may take place according to glycemic control

Locations

Country Name City State
Israel Emek medical center Afula
Israel Galilee medical center Nahariya
Israel Ziv medical center Safed
Israel Baruch Padeh Medical center, Poriya Tiberias North

Sponsors (1)

Lead Sponsor Collaborator
The Baruch Padeh Medical Center, Poriya

Country where clinical trial is conducted

Israel, 

Outcome

Type Measure Description Time frame Safety issue
Primary Mean maternal daily glucose values According to daily glucose charts Up to 4 days
Primary The rate of neonatal hypoglycemia in preterm deliveries (<37 gestational weeks) Up to 7 days after delivery or discharge (which ever comes first)
Secondary Mean maternal daily pre-prandial glucose values According to daily glucose charts Up to 4 days
Secondary Mean maternal daily post-prandial glucose values According to daily glucose charts Up to 4 days
Secondary Percent of abnormal values in the daily glucose chart According to daily glucose charts Up to 4 days
Secondary Rate of cesarean sections and operative deliveries At delivery
Secondary Rate of neonates who will be admitted to the neonatal intensive care unit APGAR scale of 0-worst and 10-best Up to a week after delivery
Secondary Apgar score at 1 and 5 minutes At delivery
Secondary Cord blood pH levels (when taken) At delivery
Secondary The rate of neonates with hyperbilirubinemia Up to 7 days after delivery or discharge (which ever comes first)
Secondary Neonatal mean head circumference Up to 7 days after delivery or discharge (which ever comes first)
Secondary Neonatal mean birth weight at delivery
Secondary The rate of fetal malformations and developmental disorders Up to 7 days after delivery or discharge (which ever comes first)
Secondary Mean and lowest neonatal blood glucose values in preterm neonates Up to 7 days after delivery or discharge (which ever comes first)
Secondary The rate of maternal adverse effects 48 hours
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