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Intrapartum Maternal Glycemic Control Using Insulin Pump Versus Insulin Drip - Cohort Observational Trial

Intrapartum Maternal Glycemic Control Using Insulin Pump Versus Insulin Drip Cohort Retrospective and Prospective Observational Trial

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01158040
Enrollment
88
Registered
2010-07-08
Start date
2010-08-31
Completion date
2012-08-31
Last updated
2010-07-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Pregestational Diabetes

Keywords

Maternal intrapartum glycemic control, Pregestational diabetes

Brief summary

The purpose of this study is to compare intrapartum glycemic control using insulin pump versus intravenous (IV) insulin administration.

Detailed description

Intrapartum maternal glycemic control in women suffering from pregestational diabetes mellitus type 1 will be evaluated and compared in the 3 study groups. Maternal and neonatal capillary blood glucose will be measured. All women suffering from diabetes mellitus and all neonates to hyperglycemic mothers are being tested for their blood glucose in our institute. Measurements' data will be collected. The primary outcome of the study is the number of neonatal hypoglycemic events (neonatal blood glucose \< 40mg/dL). All women participating in the study will be treated according to the standard accepted protocol for the treatment of pregestational diabetes during labor in our institute. The research will not include new treatments or equipment. The study is a cohort prospective and retrospective observational study in the tertiary center - Sheba medical center.

Interventions

None listed

Sponsors

Sheba Medical Center
Lead SponsorOTHER_GOV

Study design

Observational model
COHORT

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 50 Years
Healthy volunteers
Yes

Inclusion criteria

* Pregnant women suffering from pregestational diabetes mellitus type-1, * Women are being treated for a minimum of 3 months in the high risk pregnancy clinic in Sheba medical center * Women are being treated with either insulin pump or SC insulin (basal-bolus)

Exclusion criteria

* Women not compliant to treatment * Women not planning their delivery in our institute

Design outcomes

Primary

MeasureTime frameDescription
Neonatal hypoglycemia (neonatal capillary blood glucose lowers then 40 mg/dL)Up to 2 hours postpartumAll neonates to mothers who suffer from diabetes mellitus are being routinely tested for neonatal hypoglycemia in our department. Their capillary blood glucose level is being tested in the first 2 hours postpartum. Data will be gathered and compared in women being treated with insulin pump during labor versus women being treated with IV insulin

Secondary

MeasureTime frameDescription
Mean maternal blood glucose during laborOver the course of deliveryAll women suffering from pregestational diabetes mellitus are being routinely tested for blood glucose levels during delivery in our department. Their capillary blood glucose level is being tested every 1 hour throughout the active phase of delivery. Mean maternal blood glucose during partum will be compared in women being treated with insulin pump during labor versus women being treated with IV insulin

Countries

Israel

Contacts

Primary ContactHagit Shani, MD
shani.hagit@gmail.com972-50-7509442
Backup ContactRakefet Yoeli-Ulman, MD
rakefety@bezeqint.net972-54-6551819

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026