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Beneficial Effects of Antenatal Magnesium Sulfate (BEAM Trial)

Phase 3
Completed
Conditions
Periventricular Leukomalacia
Intraventricular Hemorrhage
Cerebral Palsy
Abruptio Placentae
Pulmonary Edema
Registration Number
NCT00014989
Lead Sponsor
The George Washington University Biostatistics Center
Brief Summary

As many more premature infants survive, the numbers of these infants with health problems increases. The rate of cerebral palsy (CP) in extremely premature infants is approximately 20%. Magnesium sulfate, the most commonly used drug in the US to stop premature labor, may prevent CP. This trial tests whether magnesium sulfate given to a woman in labor with a premature fetus (24 to 31 weeks out of 40) will reduce the rate of death or moderate to severe CP in the children at 2 years. The children receive ultrasounds of their brains as infants and attend three follow-up visits over two years to assess their health and development.

Detailed Description

The prevalence of cerebral palsy is increasing as the survival rate of extremely premature infants is improving. Studies have suggested an apparent association between maternal magnesium sulfate administration and a reduced risk of cerebral palsy. Other studies have suggested a possible association between magnesium sulfate and a reduction in neonatal cranial ultrasound abnormalities which may be markers for subsequent development of cerebral palsy.

This multicenter trial tests whether prophylactic magnesium sulfate given to women, for whom preterm delivery is imminent, reduces the risk of death or moderate to severe cerebral palsy in their children. Women presenting from 24.0 to 31.6 weeks gestation with advanced preterm labor or premature rupture of the membranes (pPROM) and no recent exposure to magnesium sulfate are randomized to receive either intravenous magnesium sulfate or masked study drug placebo. The study drug is administered as a 6 gram loading dose followed by a 2 gram/hour infusion (or equivalent rate for placebo). If after 12 hours, delivery has not occurred and is not anticipated, the infusion is stopped. No other parenteral tocolytics other than the IV medication may be used. Retreatment with study medication is given any time labor recurs or delivery is anticipated until gestational age is \> 34.0 wks. Standard clinical management and therapy is to be maintained for all study patients. Patients are assessed for signs of intolerance to the study medications and maternal data are collected up to hospital discharge. A sample of venous blood is collected and neonatal cranial ultrasounds are performed. Up to three follow-up visits are scheduled over two years where certified examiners, masked to study group assignment, collect physical and neurological data, including a modified Gross Motor Function Classification Scale. The Bayley Scales of Infant Development is also administered. Cranial ultrasounds are reviewed centrally.

The primary outcome is a composite outcome of death or moderate to severe cerebral palsy. Secondary outcomes include maternal infectious morbidity, pulmonary edema and placental abruption, neonatal stillbirth and death, intraventricular hemorrhage, periventricular leukomalacia, neonatal infectious and noninfectious morbidity.

Recruitment & Eligibility

Status
COMPLETED
Sex
Female
Target Recruitment
2136
Inclusion Criteria
  • Pregnant with diagnosis of preterm labor
  • Membrane rupture or delivery definitely planned within 24 hours
  • Gestational age > 24.0 and < 31.6 wks, viable fetus
Exclusion Criteria
  • Prior IV magnesium sulfate therapy within 12 hours of screening
  • Delivery expected <2 hrs
  • Cervical dilation > 8 cm
  • More than 2 fetuses
  • Known major fetal anomalies
  • Hypertension or preeclampsia
  • Maternal medical complications contraindicating magnesium sulfate treatment
  • Participation in any intervention study which influences infant neurological outcome
  • Previous participation in this trial

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Primary Outcome Measures
NameTimeMethod
Composite outcome of death or moderate to severe cerebral palsy
Secondary Outcome Measures
NameTimeMethod
Placental abruption
Birth weight
Neonatal infectious morbidity
Maternal
Pulmonary edema
Neonatal
Neonatal noninfectious morbidity
Endometritis
Other infectious morbidity
Stillbirth and neonatal death
Intraventricular hemorrhage
Days in NICU
Chorioamnionitis

Trial Locations

Locations (17)

Case Western University

🇺🇸

Cleveland, Ohio, United States

University of Texas Medical Branch - Galveston

🇺🇸

Galveston, Texas, United States

MCP Hahnemann University

🇺🇸

Philadelphia, Pennsylvania, United States

Dept of OB/GYN, Southwestern Medical Center, University of Texas

🇺🇸

Dallas, Texas, United States

University of Alabama

🇺🇸

Birmingham, Alabama, United States

Dept of OB/GYN, Hutzel Hospital

🇺🇸

Detroit, Michigan, United States

University of Utah Medical Center

🇺🇸

Salt Lake City, Utah, United States

Northwestern University

🇺🇸

Chicago, Illinois, United States

Dept of OB/GYN, Ohio State University

🇺🇸

Columbus, Ohio, United States

Women and Infants Hospital

🇺🇸

Providence, Rhode Island, United States

St. Luke's - Roosevelt Hospital

🇺🇸

New York, New York, United States

University of Texas - Houston

🇺🇸

Houston, Texas, United States

The University Hospital, University of Cincinnati

🇺🇸

Cincinnati, Ohio, United States

Dept of OB/GYN, University of Miami

🇺🇸

Miami, Florida, United States

Forsyth Memorial Hospital, Wake Forest University School of Medicine

🇺🇸

Winston-Salem, North Carolina, United States

University of North Carolina

🇺🇸

Chapel Hill, North Carolina, United States

Dept of OB/GYN Magee Womens Hospital

🇺🇸

Pittsburgh, Pennsylvania, United States

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