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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02912091
Other study ID # 21014
Secondary ID
Status Completed
Phase N/A
First received September 21, 2016
Last updated September 7, 2017
Start date August 2012
Est. completion date January 2014

Study information

Verified date September 2017
Source St. Louis University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

This study will look at blood sugar levels in pregnant women who have been given a glucocorticoid (steroid) medication to enhance fetal lung maturity. The findings will help determine the likelihood, predictive value, adverse effects, response of patients diagnosed with gestational diabetes and time course of blood sugar elevation following steroids.


Description:

The investigators hypothesize that maternal glucose levels will be elevated in the first 72 hours after steroid administration, and that the magnitude of the peak will be predictive of a diagnosis of gestational diabetes. This is a retrospective chart review.


Recruitment information / eligibility

Status Completed
Enrollment 200
Est. completion date January 2014
Est. primary completion date January 2014
Accepts healthy volunteers No
Gender Female
Age group 14 Years to 50 Years
Eligibility Inclusion Criteria:

- Intrauterine pregnancy at 22 weeks to 36 weeks gestation at time of steroid administration

- Singleton

- Patient receiving antenatal corticosteroid course for fetal lung maturity consisting of betamethasone or dexamethasone

- Age range: 14yo-50yo W-omen without known gestational diabetes and women with non-insulin requiring gestational diabetes (A1GDM)

Exclusion Criteria:

- Women with known gestational diabetes (diagnosed before steroid administration) that has required insulin or other medical therapy to control

- Women with overt diabetes which predates pregnancy.

- Chronic terbutaline therapy or other concurrent chronic beta-adrenergic agonist use

- Patients on parenteral or oral corticosteroids for reasons other than to improve -fetal lung maturity

- Multiple gestation

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
St. Louis University

Outcome

Type Measure Description Time frame Safety issue
Primary Time To determine the length of time that maternal glucose levels remain elevated after steroid administration. length of time that maternal glucose levels remain elevated
Secondary Peak glucose levels To determine when the peak glucose levels occur, the magnitude of the peak glucose, and whether either predicts a future diagnosis of gestational diabetes varies
Secondary Diet controlled To determine the corresponding response of blood glucose for patients with known gestational diabetes who are currently diet-controlled and if diagnosis of gestational diabetes can be made based upon the maternal response to steroid administration. varies
Secondary Newborn To determine any effects of maternal glucose elevation on the newborn. varies
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