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Clinical Trials/NCT01158040
NCT01158040UnknownNot Applicable

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

Sheba Medical Center1 site in 1 country88 target enrollmentStarted: August 2010Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Enrollment
88
Locations
1
Primary Endpoint
Neonatal hypoglycemia (neonatal capillary blood glucose lowers then 40 mg/dL)

Study Overview

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.

Study Design

Study Type
Observational
Observational Model
Cohort

Eligibility Criteria

Ages
18 Years to 50 Years (Adult)
Sex
Female
Accepts 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

Outcomes

Primary Outcomes

Neonatal hypoglycemia (neonatal capillary blood glucose lowers then 40 mg/dL)

Time Frame: Up to 2 hours postpartum

All 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 Outcomes

  • Mean maternal blood glucose during labor(Over the course of delivery)

Investigators

Sponsor Class
Other Gov

Study Sites (1)

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