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CompletedNCT00337142Updated Jun 30, 2009

Follow up Glucose Levels Among Infants of Diabetic Mothers

An observational study in Newborn, Full Term and Diabetic Mother, sponsored by Sheba Medical Center. Completed. Open to participants aged 1 Day to 1 Day. Per ClinicalTrials.gov, last updated 2009-06-30.

Sponsored by Sheba Medical Center · Observational

Study type
Observational
Model
Cohort
Time perspective
Retrospective
Enrollment
250
Ages
1 Day to 1 Day
Sex
All
01

Study summary

Infants to diabetic mothers (IDM) are at risk for developing hypoglycemia after birth. Glucose level follow ups are recommended to each IDM. However, there are no recommendations as to how long this follow up should be performed for, nor are there "safe" glucose levels that allow stopping glucose monitoring.

The aim of the study is to retrospectively follow up glucose levels among IDMs in order to find risk factors for developing hypoglycemia and determine time and glucose levels that would permit monitoring cessation.

Read the detailed description

A retrospective study of 250-300 IDMs, born in a single large medical center. Data will be collected as follows: Gestational age, birth weight, sex, delivery mode, type of maternal diabetes, other maternal diseases, feeding mode. Glucose levels as were recorded according to newborn protocol (1,2,4,6 hours after delivery, and then every 8 hours for total of 48 hours). Data of hypoglycemia treatment, if given, will be collected.

Later we will statistically try to determine the risk factors for developing hypoglycemia and the "safe" time and glucose levels to stop monitoring.

02

Conditions studied

  • Newborn
  • Full Term
  • Diabetic Mother

Keywords

  • gestational diabetes
  • newborn
  • hypoglycemia
03

In context

Lead sponsor

Sheba Medical Center is the lead sponsor of 660 studies on the registry; 63 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
1 Day to 1 Day
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

primary care clinic

Inclusion criteria

  • Full-term infants, diabetic mothers, Singleton

Exclusion criteria

Exclusion Criteria:

  • Preterm infants, multiple pregnancy, congenital malformations, clinically ill at birth.
05

Study design

Observational model
Cohort
Time perspective
Retrospective
Enrollment
250 participants (estimated)
06

Study locations

No study locations are listed for this record.

07

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jun 30, 2009, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
08

Registry details

Key details

Study ID
NCT00337142
Lead sponsor
Sheba Medical Center
First posted
Jun 15, 2006
Start date
Jun 2006
Primary completion
Dec 2006
Completion
Dec 2006
Last update
Jun 30, 2009

Study contacts

Ayala Maayan, MD
principal investigator · Sheba Medical Center
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Jun 2009. You cannot join it, but the record below documents what was studied.

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