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
About this trial
This is an interventional treatment trial for Diabetes focused on measuring Gestational Diabetes,, Insulin,, Glyburide,, Glycemia
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
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
NCT ID
NCT01731431
First Posted
September 11, 2012
Last Updated
December 7, 2017
Sponsor
Assistance Publique - Hôpitaux de Paris
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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