Acarbose and Prandial Insulin for the Treatment of Gestational Diabetes Mellitus. (ACARB-GDM)

Assistance Publique - Hôpitaux de Paris

Status and phase: Terminated; Phase 3

Conditions: Gestational Diabetes Mellitus in Pregnancy

Treatments: Drug: Acarbose; Drug: Prandial insulin

Study type: Interventional

Funder types: Other

Identifiers

NCT03380546

P150942

Details and patient eligibility

About

Caring for women with gestational diabetes mellitus (GDM) is very time-consuming. Therapeutic strategy includes dietary and lifestyle measures and additional insulin therapy for 15 to 40% of the women with GDM if the glycemic targets are not achieved after a period of 1 to 2 weeks of diet. Insulin therapy is imperfect for the following main reasons: need for education (i.e. subcutaneous administration, dose titration), hypoglycemia and weight gain, limited acceptance and high cost. Psychosocial deprivation is associated with more cases of GDM and health accessibility may be unequal.

Glucosidase inhibitors (acarbose) reduce intestinal absorption of starch and reduce the rate of complex carbohydrate digestion. It mainly lowers postprandial glucose values and is used in type 2 diabetes for a long time. Less than 2% of a dose is absorbed as active drug in adults, with 34% of the metabolites found in the systemic circulation. Doses of up to 9 and 32 times the human dose were not teratogenic in pregnant rats or rabbits. Limited but reassuring data during pregnancy are available. Acarbose was well tolerated (little gestational weight gain, no hypoglycemia) with digestive discomfort in some women, balanced by treatment satisfaction as compared with insulin injections. Our hypothesis is that treatment aiming to control postprandial glucose values with acarbose as compared with prandial insulin injection will be as efficient and safe, but more convenient and less expensive.

Full description

Phase III study. Prospective, multicenter, non-inferiority, randomized, open-labelled and controlled study with two arms.

1. In the 37 participating hospitals: selection of women with GDM who have unmet post prandial glycemic targets between 14 and 37 (+6 days) weeks of amenorrhea after at least 7 days of dietary and lifestyle measures. They may be treated with basal insulin to control pre prandial glucose values.

2. Explanation of protocol, with signature of consent in case of acceptation.

3. Randomization

   . Experimental group: The women will receive acarbose with a progressive increase of dose according to post prandial glucose values and digestive tolerance, with a maximal dose of 3 x 100 mg / day. The progressive titration of acarbose reduces gastro-intestinal side effects.

   Patients who have not reached the glycemic targets at this highest tolerated dose for at least one meal will receive instead prandial insulin therapy for each meal, whereas acarbose will be stopped. Failure to reach post-prandial target will be defined as 3 or more post-prandial glycaemic values ≥ 1.20 g/L for a given meal in a week (3 values out of 7) after the two weeks of dose adjustment.

   · Control group: The women will receive prandial insulin according to usual practice (routine care according to French recommendations): before each meal, with dose titration according to post prandial values.

   Basal insulin may be necessary in both arms to control pre-prandial glucose values.

   At delivery:

   • Maternal blood samples : 14 ml of blood will be collected at the same time as the sample routinely collected just before delivery for irregular agglutinin test measurement, when the women are perfused.

   • Cord fluid : 7 ml will be collected at the same as cord fluid pH is routinely measured just after delivery. There will be 5 aliquots to prepare.

   The aliquots previously labelled and stowed in the specific boxes for the study will be stored locally and will be transported to the "Centre de Ressources Biologiques"(CRB) of the Jean Verdier Hospital.

4. Routine monitoring of the women with GDM in both arms, up to delivery. No use of other oral hypoglycemic agents during pregnancy.

5. Last consultation three months after delivery.

Enrollment: 341 patients

Sex: Female

Ages: 18 to 45 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Age ≥ 18 years
• Singleton pregnancy
• GDM diagnosed during pregnancy according to IADPSG criteria
• Self-monitoring of blood glucose
• After at least 7 days of dietary and lifestyle measures, unreached post-prandial glucose control
• 14-37 (+ 6 days) amenorrhea weeks at the time of randomization
• Signed informed consent

Exclusion criteria

• Prandial insulin use before randomization during this pregnancy
• Use of other oral hypoglycemic agents during this pregnancy
• Multiple pregnancy
• Known hepatic insufficiency
• Long time corticosteroid treatment
• Pre-existing diabetes in pregnancy
• Overt diabetes diagnosed during pregnancy (IADPSG criteria)
• Lack of Social Insurance
• Insufficient understanding
• Participant in another investigational drug study at inclusion visit
• Contraindications of acarbose
• Fetal malformation diagnosed by previous fetal ultrasound

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: None (Open label)

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341 participants in 2 patient groups

acarbose

Experimental group

Description:

The women will receive acarbose with a progressive increase of dose according to post prandial glucose values and digestive tolerance, with a maximal dose of 3 x 100 mg /day

Treatment:

Drug: Acarbose

prandial insulin

Active Comparator group

Description:

The women will receive prandial insulin according to usual practice (routine care according to French recommendations): before each meal, with dose titration according to post prandial values.

Treatment:

Drug: Prandial insulin