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Completed No phase listed Observational Accepts healthy volunteers

In Utero Magnesium Sulfate Exposure: Effects on Extremely-Low-Birth-Weight Infants

ClinicalTrials.gov ID: NCT01203501

Public ClinicalTrials.gov record NCT01203501. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Sep 6, 2026, 6:39 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

In Utero Magnesium Sulfate Exposure: Effects on Extremely-Low-Birth-Weight (ELBW) Infants

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

This study examined the effect of magnesium sulfate (MgSO4) exposure on adverse outcome in extremely low birth weight (ELBW) infants. For infants included in the NICHD Neonatal Research Network Generic Database whose mothers were given prenatal MgSO4, data were prospectively collected on maternal/infant conditions and magnesium exposure (including indications, timing and duration of exposure).

Study identification

NCT ID
NCT01203501
Recruitment status
Completed
Study type
Observational
Phase
Not listed
Enrollment
1,339 participants

Conditions and interventions

Eligibility (public fields only)

Age range
Up to 14 Days
Sex
All
Healthy volunteers
Accepts healthy volunteers

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Jun 30, 1996
Primary completion
May 31, 1998
Completion
May 31, 2000
Last update posted
Sep 25, 2017

1996 – 2000

United States locations

U.S. sites
15
U.S. states
14
U.S. cities
15
Facility City State ZIP Site status
University of Alabama at Birmingham Birmingham Alabama 35233
Stanford University Palo Alto California 94304
Yale University New Haven Connecticut 06504
George Washington University Washington D.C. District of Columbia 20052
University of Miami Miami Florida 33136
Emory University Atlanta Georgia 30303
Indiana University Indianapolis Indiana 46202
Harvard University Cambridge Massachusetts 02138
Wayne State University Detroit Michigan 48201
University of New Mexico Albuquerque New Mexico 87131
Cincinnati Children's Medical Center Cincinnati Ohio 45267
Case Western Reserve University, Rainbow Babies and Children's Hospital Cleveland Ohio 44106
Brown University, Women & Infants Hospital of Rhode Island Providence Rhode Island 02905
University of Tennessee Memphis Tennessee 38163
University of Texas Southwestern Medical Center at Dallas Dallas Texas 75235

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01203501, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Sep 25, 2017 · Synced Sep 6, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01203501 live on ClinicalTrials.gov.

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