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Glycemic Profile in Women With Gestational Diabetes Treated With Glyburide

Primary Purpose

Gestational Diabetes

Status
Withdrawn
Phase
Phase 4
Locations
United States
Study Type
Interventional
Intervention
Glyburide
Continuous glucose monitor
Sponsored by
University of Pittsburgh
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Gestational Diabetes

Eligibility Criteria

18 Years - 50 Years (Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria:

  • Pregnant women with gestational diabetes
  • Singleton gestation
  • Receiving glyburide for the treatment gestational diabetes
  • Able to give consent

Exclusion Criteria:

  • Women who require insulin for the treatment of gestational diabetes
  • Diagnosis of pregestational diabetes
  • Poor glycemic control, > 50% of blood glucose values over 200mg/dl prior to start of the study
  • Women receiving medications that affect glycemic control e.g. steroids, within a week of enrollment.

Sites / Locations

  • Magee Womens Hospital of UPMC

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Experimental

Experimental

Experimental

Arm Label

Glyburide once daily

Glyburide twice daily

Mixed meal tolerance test.

Arm Description

Timing of glyburide dosing will be changed, glucose will be monitored using continuous a glucose monitor.

Dose interval and timing of glyburide dose will be changed, glucose will be monitored using continuous a glucose monitor.

Subjects will be admitted to the Clinical Translational Research Center, receive a Mixed meal tolerance test and have timed blood draws to assess the effect of glyburide on glucose and insulin metabolism.

Outcomes

Primary Outcome Measures

Glucose levels throughout the day

Secondary Outcome Measures

Full Information

First Posted
September 17, 2013
Last Updated
May 10, 2016
Sponsor
University of Pittsburgh
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1. Study Identification

Unique Protocol Identification Number
NCT01947699
Brief Title
Glycemic Profile in Women With Gestational Diabetes Treated With Glyburide
Study Type
Interventional

2. Study Status

Record Verification Date
May 2016
Overall Recruitment Status
Withdrawn
Why Stopped
PI decided to withdrawal study before recruitment started
Study Start Date
September 2013 (undefined)
Primary Completion Date
September 2014 (Actual)
Study Completion Date
September 2014 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Pittsburgh

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Diabetes is more likely to occur during pregnancy. When present only in pregnancy it is called gestational diabetes, and it places both mom and baby at risk for complications. Glyburide is one of the currently used treatments for diabetes during pregnancy. This drug is a medication taken by mouth that decreases sugar levels in the blood. It is known to decrease the risk of complications linked to diabetes in pregnancy. Recent studies in pregnancy have described a difference in the way and how well the drug works compared to when used outside of pregnancy. Oral blood sugar lowering agents are approved by the Food and Drug Administration (FDA) to lower blood sugar in non-pregnant subjects with diabetes. No oral (taken by mouth) blood-sugar lowering agents are FDA approved for use in pregnancy. Although Glyburide is not FDA approved for this use, it is the most commonly used oral blood sugar lowering agent in pregnancy. This research study will help us learn more about the variations in blood sugar levels in women with diabetes in pregnancy who are taking glyburide and how changes in the timing of when the glyburide is taken would affect blood glucose levels. The goals of this study are: To find the how glucose changes throughout the day in women with diabetes in pregnancy receiving glyburide To learn the effect of changing the time of taking glyburide on glucose levels To learn the effect of changing the time between glyburide doses on glucose levels To see if insulin is secreted the same throughout the day in response to a morning dose of glyburide.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Gestational Diabetes

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
0 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Glyburide once daily
Arm Type
Experimental
Arm Description
Timing of glyburide dosing will be changed, glucose will be monitored using continuous a glucose monitor.
Arm Title
Glyburide twice daily
Arm Type
Experimental
Arm Description
Dose interval and timing of glyburide dose will be changed, glucose will be monitored using continuous a glucose monitor.
Arm Title
Mixed meal tolerance test.
Arm Type
Experimental
Arm Description
Subjects will be admitted to the Clinical Translational Research Center, receive a Mixed meal tolerance test and have timed blood draws to assess the effect of glyburide on glucose and insulin metabolism.
Intervention Type
Drug
Intervention Name(s)
Glyburide
Intervention Type
Device
Intervention Name(s)
Continuous glucose monitor
Primary Outcome Measure Information:
Title
Glucose levels throughout the day
Time Frame
One week

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
50 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Pregnant women with gestational diabetes Singleton gestation Receiving glyburide for the treatment gestational diabetes Able to give consent Exclusion Criteria: Women who require insulin for the treatment of gestational diabetes Diagnosis of pregestational diabetes Poor glycemic control, > 50% of blood glucose values over 200mg/dl prior to start of the study Women receiving medications that affect glycemic control e.g. steroids, within a week of enrollment.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Maisa Feghali, MD
Organizational Affiliation
University of Pittsburgh
Official's Role
Principal Investigator
Facility Information:
Facility Name
Magee Womens Hospital of UPMC
City
Pittsburgh
State/Province
Pennsylvania
ZIP/Postal Code
15213
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
19295505
Citation
Hebert MF, Ma X, Naraharisetti SB, Krudys KM, Umans JG, Hankins GD, Caritis SN, Miodovnik M, Mattison DR, Unadkat JD, Kelly EJ, Blough D, Cobelli C, Ahmed MS, Snodgrass WR, Carr DB, Easterling TR, Vicini P; Obstetric-Fetal Pharmacology Research Unit Network. Are we optimizing gestational diabetes treatment with glyburide? The pharmacologic basis for better clinical practice. Clin Pharmacol Ther. 2009 Jun;85(6):607-14. doi: 10.1038/clpt.2009.5. Epub 2009 Mar 18.
Results Reference
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PubMed Identifier
23812467
Citation
Caritis SN, Hebert MF. A pharmacologic approach to the use of glyburide in pregnancy. Obstet Gynecol. 2013 Jun;121(6):1309-1312. doi: 10.1097/AOG.0b013e31829007f0.
Results Reference
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Learn more about this trial

Glycemic Profile in Women With Gestational Diabetes Treated With Glyburide

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