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Magnesium Sulfate For Brain Injury

This study has been completed.

Sponsored by: National Institute of Neurological Disorders and Stroke (NINDS)
Information provided by: National Institute of Neurological Disorders and Stroke (NINDS)
ClinicalTrials.gov Identifier: NCT00004730
  Purpose

The purpose of the study is to determine whether magnesium sulfate, given within 8 hours of a moderate or severe traumatic brain injury improves survival, decreases the number of people developing seizures, improves the survivors' mental and psychological functioning, including the ability to return to daily life, live independently, and return to work or school.


Condition Intervention Phase
Brain Injuries
Head Injury
Brain Concussion
Drug: magnesium sulfate
Phase III

MedlinePlus related topics:   Concussion    Injuries    Traumatic Brain Injury    Wounds   

Drug Information available for:   Magnesium    Magnesium sulfate   

U.S. FDA Resources

Study Type:   Interventional
Study Design:   Treatment, Randomized, Double-Blind, Placebo Control, Parallel Assignment
Official Title:   Magnesium Sulfate for Neuroprotection After Brain Trauma

Further study details as provided by National Institute of Neurological Disorders and Stroke (NINDS):

Study Start Date:   August 1999

Detailed Description:

The purpose of the study is to determine if treating head-injured patients with magnesium sulfate will improve medical, mental, and psychological recovery. In particular, the study will assess each patient's ability to return to daily life, live independently, and return to work or school as done before the head injury occurred. The study will also assess magnesium sulfate's ability to reduce the risk of developing seizures (epilepsy) as well as to improve survival rates after a traumatic brain injury. Patients on the study are assigned randomly (by chance) to either the magnesium sulfate group or the group which gets a placebo. This means they have an equal chance of being in either group. Before the first dose is given, two teaspoons worth of blood are drawn from a vein in the arm. The first dose of magnesium sulfate is 1meq/kg given intravenously within 8 hours of injury. Then a five day continuous intravenous infusion of magnesium sulfate 0.24meq/kg per hour is begun. Daily magnesium levels are checked and the dose changed in order to keep the Magnesium blood level at approximately 4meq/L. If the person does not receive magnesium sulfate, he receives a placebo which looks just like magnesium sulfate but contains no active medication. If the person leaves the hospital before the five days are over, the magnesium or placebo is stopped. Patients on the study will receive a brief exam in person or over the phone at one and three months after the injury to determine whether they have had any seizures and to evaluate how they are functioning and recovering from their head injury. Each evaluation will last about one hour. At six months after the injury, they will have full neuropsychological and psychosocial evaluations done at Harborview. These tests will take about five hours to complete and include tests of vocabulary, problem solving, and coordination. There will be questions about how the injury has affected the way they feel and interact socially. For example, there will be questions about their ability to work, manage personal affairs, what their moods are like, and how anger is handled.

  Eligibility
Ages Eligible for Study:   14 Years and older
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No

Criteria

Inclusion Criteria:

  • Traumatic brain injury with post-resuscitation Glasgow Coma Scale of 3-12 or, if intubated, motor score of 1-5, or who require emergent neurosurgical intervention precluding the accurate assessment of Glasgow Coma Scale.

Exclusion Criteria:

  • Injury greater than 8 hours old
  • Age under 14 years
  • Compromised renal function (creatinine of 2.0 mb/dl or greater)
  • Membership in a vulnerable population (e.g. pregnant woman, prisoner, etc.)
  • Residence making follow-up unlikely (e.g. lives outside U.S.)
  • Refusal to participate
  Contacts and Locations

Please refer to this study by its ClinicalTrials.gov identifier: NCT00004730

Locations
United States, Washington
University of Washington    
      Seattle, Washington, United States, 98104

Sponsors and Collaborators

Investigators
Principal Investigator:     Nancy Temkin, Ph.D.     University of Washington    
  More Information


Study ID Numbers:   R01NS19643
First Received:   February 25, 2000
Last Updated:   July 21, 2006
ClinicalTrials.gov Identifier:   NCT00004730
Health Authority:   United States: Federal Government

Keywords provided by National Institute of Neurological Disorders and Stroke (NINDS):
head injury  
traumatic brain injury  
concussion  
magnesium sulfate  
neuroprotection  

Study placed in the following topic categories:
Craniocerebral Trauma
Brain Concussion
Magnesium Sulfate
Wounds and Injuries
Disorders of Environmental Origin
Head Injuries, Closed
Central Nervous System Diseases
Wounds, Nonpenetrating
Trauma, Nervous System
Brain Diseases
Brain Injuries

Additional relevant MeSH terms:
Molecular Mechanisms of Pharmacological Action
Nervous System Diseases
Physiological Effects of Drugs
Calcium Channel Blockers
Anesthetics
Central Nervous System Depressants
Reproductive Control Agents
Cardiovascular Agents
Pharmacologic Actions
Membrane Transport Modulators
Tocolytic Agents
Sensory System Agents
Therapeutic Uses
Analgesics
Peripheral Nervous System Agents
Anti-Arrhythmia Agents
Central Nervous System Agents
Anticonvulsants

ClinicalTrials.gov processed this record on December 03, 2008




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