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Multicenter Randomized Trial of Non-inferiority Between Glyburide and Insulin for the Treatment of Gestational Diabetes (INDAO)

Primary Purpose

Diabetes, Gestational

Status
Completed
Phase
Phase 3
Locations
France
Study Type
Interventional
Intervention
Insulin
Glyburide
Sponsored by
Assistance Publique - Hôpitaux de Paris
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Diabetes focused on measuring Gestational Diabetes,, Insulin,, Glyburide,, Glycemia

Eligibility Criteria

18 Years - 45 Years (Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria:

  • gestational diabetes diagnosed between 24 and 34 weeks according to international criteria.

Exclusion Criteria:

  • Multiple Pregnancy
  • Chronic Hypertension
  • Preeclampsia
  • Renal impairment
  • Hepatic insufficiency
  • Long time corticosteroids treatment
  • Allergy to sulfa drugs
  • Pre-existing diabetes in pregnancy
  • Abnormal result on screening test for gestational diabetes before 24SA
  • Fasting glucose ≥ 1.26 g / l at initial diagnosis of diabetes
  • The need for drug treatment contraindicated or not recommended with taking Glibenclamide
  • Poor understanding of French
  • Lack of Social Insurance

Sites / Locations

  • Marie-Victoire Senat

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Experimental

Arm Label

Insulin

Glyburide

Arm Description

standard protocol of insulin treatment for gestational diabetes

initial dose 2.5 mg per day increased if necessary until 10mg twice a day if glycemia is not controlled

Outcomes

Primary Outcome Measures

Composite criterion of neonatal complications associated with gestational diabetes: macrosomia or birth weight ≥ 90th percentile for gestational age, neonatal hypoglycemia and neonatal hyperbilirubinemia

Secondary Outcome Measures

Rates of caesarean section, preterm delivery rate, neonatal mortality rate, number of neonatal and maternal trauma related to delivery, number of respiratory distress, number of prenatal visits, number of days of hospitalization
Maternal glycemic control, rates of caesarean section, preterm delivery rate, neonatal mortality rate, number of neonatal and maternal trauma related to delivery, number of respiratory distress, number of prenatal visits, number of days of hospitalization and maternal satisfaction

Full Information

First Posted
September 11, 2012
Last Updated
December 7, 2017
Sponsor
Assistance Publique - Hôpitaux de Paris
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1. Study Identification

Unique Protocol Identification Number
NCT01731431
Brief Title
Multicenter Randomized Trial of Non-inferiority Between Glyburide and Insulin for the Treatment of Gestational Diabetes
Acronym
INDAO
Official Title
Multicenter Randomized Trial of Non-inferiority Between Glyburide and Insulin for the Treatment of Gestational Diabetes
Study Type
Interventional

2. Study Status

Record Verification Date
December 2017
Overall Recruitment Status
Completed
Study Start Date
May 18, 2012 (Actual)
Primary Completion Date
March 15, 2017 (Actual)
Study Completion Date
June 2, 2017 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Assistance Publique - Hôpitaux de Paris

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
This clinical trial aims to test whether glibenclamide is non-inferior to insulin for the treatment of gestational diabetes.
Detailed Description
In patients with gestational diabetes, a therapeutic treatment with a diet, a blood glucose monitoring and, if necessary, treatment with insulin is associated with reduced neonatal complications. Although the effectiveness of insulin is proven, this therapy has many drawbacks, especially in terms of implementation and monitoring by women. An alternative is the use of oral antidiabetic agents like glibenclamide. Assumption: Glibenclamide is non-inferior to insulin for the treatment of gestational diabetes. Main objective: To test the oral Glibenclamide is non-inferior to subcutaneous insulin for the occurrence of perinatal complications in the management of pregnant women developing gestational diabetes and requiring treatment other than dietary. Secondary Objective: To test the noninferiority of two treatments on maternal glycemic control and maternal complications. Sample size: With a 80% power and a significance level of 5%, 450 subjects per group are required to show that treatment with glibenclamide is not considered inferior to treatment with insulin if the frequency of outcome composite does not exceed 25% with glibenclamide, whereas it was 18% with insulin (calculated with a non-inferiority margin of 7% and considering that 20% of patients treated with glyburide and Insulin for change half of the patients accept randomization). Progress of the study: Inclusion of women between 24 and 34 weeks. Randomization between Insulin and Glibenclamide after failure of 10 days of dietary treatment well done. Failure defined by at least 2 abnormal values of glycemia: fasting glucose ≥ 0.95 g / l and/or a postprandial 2h ≥ 1.20 g / l. Women will receive either insulin according to the usual protocol or Glibenclamide at an initial dose of 2.5 mg / once daily in the morning before breakfast. So long as the glycemic targets will not be reached doses are gradually increased stepwise every 4 days until day 21 (20mg/j) . Patients who have not reached the glycemic targets at this highest dose will have a change in treatment for insulin at day 21. Routine monitoring of pregnant women with gestational diabetes, up to a week after delivery Number of clinical sites: 15 Perspective: Use of Glibenclamide as a first line treatment of gestational diabetes requiring drug treatment.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Diabetes, Gestational
Keywords
Gestational Diabetes,, Insulin,, Glyburide,, Glycemia

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
914 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Insulin
Arm Type
Active Comparator
Arm Description
standard protocol of insulin treatment for gestational diabetes
Arm Title
Glyburide
Arm Type
Experimental
Arm Description
initial dose 2.5 mg per day increased if necessary until 10mg twice a day if glycemia is not controlled
Intervention Type
Other
Intervention Name(s)
Insulin
Intervention Type
Drug
Intervention Name(s)
Glyburide
Primary Outcome Measure Information:
Title
Composite criterion of neonatal complications associated with gestational diabetes: macrosomia or birth weight ≥ 90th percentile for gestational age, neonatal hypoglycemia and neonatal hyperbilirubinemia
Time Frame
At birth until neonatal discharge from maternity
Secondary Outcome Measure Information:
Title
Rates of caesarean section, preterm delivery rate, neonatal mortality rate, number of neonatal and maternal trauma related to delivery, number of respiratory distress, number of prenatal visits, number of days of hospitalization
Description
Maternal glycemic control, rates of caesarean section, preterm delivery rate, neonatal mortality rate, number of neonatal and maternal trauma related to delivery, number of respiratory distress, number of prenatal visits, number of days of hospitalization and maternal satisfaction
Time Frame
during pregnancy until maternal discharge from maternity

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
45 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: gestational diabetes diagnosed between 24 and 34 weeks according to international criteria. Exclusion Criteria: Multiple Pregnancy Chronic Hypertension Preeclampsia Renal impairment Hepatic insufficiency Long time corticosteroids treatment Allergy to sulfa drugs Pre-existing diabetes in pregnancy Abnormal result on screening test for gestational diabetes before 24SA Fasting glucose ≥ 1.26 g / l at initial diagnosis of diabetes The need for drug treatment contraindicated or not recommended with taking Glibenclamide Poor understanding of French Lack of Social Insurance
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Marie-Victoire SENAT, PhD
Organizational Affiliation
Assistance Publique - Hôpitaux de Paris
Official's Role
Principal Investigator
Facility Information:
Facility Name
Marie-Victoire Senat
City
Paris
ZIP/Postal Code
94270
Country
France

12. IPD Sharing Statement

Citations:
PubMed Identifier
29715355
Citation
Senat MV, Affres H, Letourneau A, Coustols-Valat M, Cazaubiel M, Legardeur H, Jacquier JF, Bourcigaux N, Simon E, Rod A, Heron I, Castera V, Sentilhes L, Bretelle F, Rolland C, Morin M, Deruelle P, De Carne C, Maillot F, Beucher G, Verspyck E, Desbriere R, Laboureau S, Mitanchez D, Bouyer J; Groupe de Recherche en Obstetrique et Gynecologie (GROG). Effect of Glyburide vs Subcutaneous Insulin on Perinatal Complications Among Women With Gestational Diabetes: A Randomized Clinical Trial. JAMA. 2018 May 1;319(17):1773-1780. doi: 10.1001/jama.2018.4072.
Results Reference
derived

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Multicenter Randomized Trial of Non-inferiority Between Glyburide and Insulin for the Treatment of Gestational Diabetes

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