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Inositol Stereoisomers to Treat Gestational Diabetes

Not Applicable
Conditions
Gestational Diabetes Mellitus
Interventions
Dietary Supplement: Myo-inositol
Dietary Supplement: Folic acid
Dietary Supplement: D-Chiro-inositol
Dietary Supplement: Myo-inositol plus D-chiro inositol
Registration Number
NCT02097069
Lead Sponsor
Università degli Studi 'G. d'Annunzio' Chieti e Pescara
Brief Summary

The investigators aim to compare the effect of different inositol stereoisomers supplementation in lowering insulin resistance levels after 8 weeks of treatment in pregnant women with GDM and in preventing adverse obstetric outcomes.

The study population includes 80 women with GDM, randomly allocated to subgroup A (folic acid 400 mcg/day), subgroup B (myo-inositol 2000 mg twice a day), subgroup C (D-chiro-inositol 250 mg twice a day), and subgroup D (Myo-inositol plus D-chiro-inositol 550mg/13,8 mg twice a day).

Folic acid or inositol stereoisomers will be administered starting at the enrolling time (24-28 week gestation, after GDM diagnosis) till the delivery.

The homeostasis model assessment of insulin resistance (HOMA-IR) and the sensitivity index (QUICKI) will be checked at the moment of the diagnostic oral glucose tolerance test (24-28 weeks) and after 8 weeks of treatment. Obstetric outcomes, the rate of women needed insulin therapy and insulin dosage will be registered.

Detailed Description

Gestational diabetes mellitus (GDM) is defined as carbohydrate intolerance that begins or is first recognized during pregnancy (1). It is characterized by an increase of physiological insulin resistance and it is associated with an increased risk of perinatal and maternal morbidity (2,3).

Inositol is a six-carbon polyol, normally present in a variety of foods, which has been classified as an insulin sensitizing agent. It exists as nine different isomers including myo-inositol (MI) and D-chiro-inositol (DCI) that are the most represented in human body. Myo-inositol and D-chiro-inositol glycans administration has been reported to exert beneficial effects at metabolic, hormonal and ovarian levels (4-5).

Recently has been demonstrated that Myo-inositol supplementation improves insulin resistance in patients with GDM (6), whereas there aren't data about the use of D-chiro-inositol or Myo-inositol plus D-chiro-inositol in women affected by GDM.

In this proposed study, the investigators aim to compare the effect of different inositol stereoisomers supplementation (Myo-inositol, D-chiro-inositol or Myo-inositol plus D-chiro-inositol ) in lowering insulin resistance levels after 8 weeks of treatment in pregnant women with GDM and in preventing adverse obstetric outcomes. All the available inositol formulations also contain folic acid (200 mcg).

The study population includes 80 women with GDM, randomly allocated to subgroup A (folic acid 400 mcg/day), subgroup B (myo-inositol 2000 mg twice a day), subgroup C (D-chiro-inositol 250 mg twice a day), and subgroup D (Myo-inositol plus D-chiro-inositol 550mg/13,8 mg twice a day).

Dietary control, folic acid or inositol stereoisomers will be administered starting at the enrolling time (24-28 week gestation, after GDM diagnosis) till the delivery.

The homeostasis model assessment of insulin resistance (HOMA-IR) and the sensitivity index (QUICKI) will be checked at the moment of the diagnostic oral glucose tolerance test (24-28 weeks) and after 8 weeks of treatment. Obstetric outcomes, the rate of women needed insulin therapy and insulin dosage will be registered.

Recruitment & Eligibility

Status
UNKNOWN
Sex
Female
Target Recruitment
80
Inclusion Criteria
  • Gestational Diabetes diagnosed within 24-28 weeks gestation
  • Caucasian pregnant women
Exclusion Criteria
  • Pre-pregnancy diabetes
  • Non-singleton pregnancy

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Subgroup BMyo-inositolmyo-inositol 2000 mg twice a day
Subgroup AFolic acidfolic acid 400 mcg/day
Subgroup CD-Chiro-inositolD-chiro-inositol 250 mg twice a day
Subgroup DMyo-inositol plus D-chiro inositolMyo-inositol plus D-chiro inositol 550mg/13,8 mg twice a day
Primary Outcome Measures
NameTimeMethod
Insulin resistance level evaluated by homeostasis model assessment of insulin resistance (HOMA-IR)56 days- 8 weeks
Secondary Outcome Measures
NameTimeMethod
cesarean sectionat delivery
neonatal hypoglycemiaat delivery
hypertensive disorders56 days- 8 weeks
macrosomiaat delivery
jaundice requiring phototherapywithin the first 2 weeks after delivery
lipid profile56 days- 8 weeks
insulin therapy requirements56 days- 8 weeks

Trial Locations

Locations (1)

Hospital "SS Annunziata"

🇮🇹

Chieti, Italy

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