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

NCT01203501 · View on ClinicalTrials.gov ↗

Study Summary

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 Locations (15)

Ohio

  • Cincinnati Children's Medical Center — Cincinnati
  • Case Western Reserve University, Rainbow Babies and Children's Hospital — Cleveland

Alabama

  • University of Alabama at Birmingham — Birmingham

California

  • Stanford University — Palo Alto

Connecticut

  • Yale University — New Haven

District of Columbia

  • George Washington University — Washington D.C.

Florida

  • University of Miami — Miami

Georgia

  • Emory University — Atlanta

Indiana

  • Indiana University — Indianapolis

Trial Details

FieldValue
Enrollment Target 1,339 participants
Start Date 1996-07
Est. Completion 2000-06

Sponsor

NICHD Neonatal Research Network

44 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT01203501

The ClinicalTrials.gov registry entry for NCT01203501 describes a study currently listed as completed. It is categorized as an unspecified phase, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 1,339 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is NICHD Neonatal Research Network, which has 44 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 7 conditions, with Cerebral Palsy appearing as the primary indexed condition, and to 0 interventions. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT01203501 reports 15 study locations spanning 14 distinct geographic areas — top geographies include Ohio, Alabama, California. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT01203501 about?

NCT01203501 is a clinical study titled "In Utero Magnesium Sulfate Exposure: Effects on Extremely-Low-Birth-Weight Infants". 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/in...

What is the current status of trial NCT01203501?

This trial is currently completed. The enrollment target is 1,339 participants. The study started on 1996-07. Estimated completion is 2000-06.

What conditions does trial NCT01203501 study?

This clinical trial studies the following conditions: Cerebral Palsy, Infant, Newborn, Infant, Premature, Infant, Small for Gestational Age, Infant, Low Birth Weight. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

Who is sponsoring clinical trial NCT01203501?

This trial is sponsored by NICHD Neonatal Research Network, which has 44 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT01203501 being conducted?

This trial has 15 study locations across Alabama, California, Connecticut, District of Columbia, Florida. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial