Magnesium Supplementation in the Second Trimester of Pregnancy to Overweight and Obese Individuals

Not Applicable

Completed

• Conditions: Gestational Diabetes; Obesity
• Interventions: Dietary Supplement: Magnesium citrate; Dietary Supplement: Placebo; Behavioral: Dietary modification

• Registration Number: NCT01510665
• Lead Sponsor: University of California, Los Angeles

Brief Summary

This is a prospective, randomized, placebo controlled study with three parallel arms examining the effects of magnesium supplementation in the second trimester of pregnancy.

Recent research has shown that supplemental magnesium can have beneficial effects, especially in overweight individuals. Not only do many people have a magnesium deficient diet, there is also evidence that magnesium can improve blood sugar levels. Due to the growing concern of obesity with pregnancy and its associated complications, such as diabetes and abnormal fetal growth, magnesium therapy could have novel and beneficial effects on pregnancy outcomes.

In this study, 60 overweight and obese pregnant patients in their first trimester will be enrolled and randomized. The first group (A) will receive oral magnesium citrate (300mg elemental Magnesium), group B will receive dietary counseling about following a magnesium rich diet from a nutritionist, and group C will receive a placebo (control). Blood and urine specimens will be collected at three time points during the pregnancy to analyze changes in levels of metabolic markers, inflammatory markers, and protein expression profiles. Fetal and maternal complications of pregnancy will be noted, including maternal weight gain. At delivery, patients will have a placental cord blood specimen and placental biopsy collected for gene expression patterns and further analysis.

Detailed Description

Not available

Basic Information
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Recruitment & Eligibility
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Study & Design
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Trial Locations

Study Timeline

• Study First Submitted: 2011-12-23
• Study Start: 2012-01
• Study First Submitted QC: 2012-01-13
• Study First Posted: 2012-01-16
• Status Verified: 2013-06
• Primary Completion: 2013-06
• Study Completion: 2013-06
• Last Update Submitted: 2013-06-12
• Last Update Posted: 2013-06-14

Recruitment & Eligibility

• Status: COMPLETED
• Sex: Female
• Target Recruitment: 28

Inclusion Criteria

• Between 18 and 40 years of age
• Pregnant in the first trimester
• Able to give informed consent
• Planning to deliver at UCLA
• BMI greater than or equal to 25

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Exclusion Criteria

• On insulin therapy or other oral hypoglycemic agents
• Multiple gestation
• Baseline HgbA1C > 6.5%
• Prior history of clinically diagnosed T2D
• Multiple dietary restrictions/food allergies
• Heart, renal, or liver failure
• Clinical history of psychiatric illness or substance abuse
• Out of town travel planned at study visits

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Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Magnesium Supplement	Magnesium citrate	Magnesium citrate dietary supplement (300 mg elemental Magnesium daily dose) given week 13 to week 28 (two pills daily)
Placebo	Placebo	Identical appearing pill with inactive ingredients given week 13 to week 28 (two pills daily)
Diet	Dietary modification	Nutritionist counseling session and advice on following a magnesium rich diet from week 13 to week 28

Primary Outcome Measures

Name	Time	Method
Change in maternal biomarkers during pregnancy up to 28 weeks	up to 28 weeks	Blood and urine markers of inflammatory and metabolic markers will be assessed during the pregnancy,comparing baseline values to second trimester values, which will be up to 28 weeks.
Neonatal birth weight/height	Up to 10 months	This measure will be assessed at neonatal delivery, which will occur at a maximum of up to 10 months from randomization. Neonatal weight and height at birth will be assessed.
Change in maternal biomarkers in pregnancy in the third trimester	Up to 36 weeks	Blood and urine markers of inflammatory and metabolic markers will be assessed during the pregnancy,comparing baseline values to third trimester values, which will be up to 36 weeks.

Secondary Outcome Measures

Name	Time	Method
Neonatal outcomes	Up to 10 months	This measure will be assessed at neonatal delivery, which will occur at a maximum of up to 10 months from randomization. At delivery, neonatal characteristics will be assessed: Macrosomia, preterm birth, head circumference, and apgar score.
Neonatal tertiary outcomes	Up to 10 months	This measure will be assessed at neonatal delivery, which will occur at a maximum of up to 10 months from randomization. Cord blood and placenta will be collected at delivery, and we will examine endothelial progenitor cell presence in cord blood, PON expression in cord blood, and DNA expression from the placental tissue.
Pregnancy complications	Up to 10 months	From date of randomization until the date of delivery of the neonate, up to a maximum of 10 months, pregnancy complications such as development of gestational diabetes, hypertension, proteinuria, shoulder dystocia, cesarean section, as well as amount of weight gain will be assessed from the chart.

Trial Locations

Locations (2)

200 Medical Plaza UCLA Ob/Gyn Clinic; 🇺🇸 Westwood, California, United States

West Medical UCLA Ob/Gyn Clinic; 🇺🇸 Westwood, California, United States