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The Use of Anti-oxidants to Reduce Sequela of Mild Traumatic Brain Injury (mTBI) After Blast Exposure

Primary Purpose

Mild Traumatic Brain Injury

Status
Completed
Phase
Not Applicable
Locations
Iraq
Study Type
Interventional
Intervention
N-acetyl-cysteine (NAC)
Placebo
Sponsored by
Brooke Army Medical Center
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Mild Traumatic Brain Injury focused on measuring mild traumatic brain injury, anti-oxidant, early treatment

Eligibility Criteria

18 Years - 50 Years (Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  1. Be active duty United States Service member
  2. Be between the ages of 18 and 50 years
  3. Present to TQ Surgical within 24 hours of blast exposure.
  4. Have complains consistent with possible TBI including hearing loss, dizziness, lightheadedness, cognitive difficulties, and/or had loss of consciousness.
  5. Are not expressly excluded by the criteria listed below.

Exclusion Criteria:

  1. Require urgent or emergent surgical procedures.
  2. Will require medical evacuation to any level III or higher facility (other then to a level III for a CT scan only).
  3. Has evidence of an open head wound.
  4. Pregnant Females
  5. The use, within the last seven days, of a nutritional supplement containing an anti-oxidant.

Sites / Locations

  • TQ Surgical

Arms of the Study

Arm 1

Arm 2

Arm Type

Placebo Comparator

Experimental

Arm Label

2

1

Arm Description

control

Active medicine

Outcomes

Primary Outcome Measures

Relief of symptoms of mTBI

Secondary Outcome Measures

Full Information

First Posted
January 13, 2009
Last Updated
August 9, 2010
Sponsor
Brooke Army Medical Center
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1. Study Identification

Unique Protocol Identification Number
NCT00822263
Brief Title
The Use of Anti-oxidants to Reduce Sequela of Mild Traumatic Brain Injury (mTBI) After Blast Exposure
Official Title
The Use of Anti-oxidants to Reduce Sequela of Mild TBI (mTBI) After Blast Exposure
Study Type
Interventional

2. Study Status

Record Verification Date
January 2009
Overall Recruitment Status
Completed
Study Start Date
November 2008 (undefined)
Primary Completion Date
March 2009 (Actual)
Study Completion Date
August 2009 (Actual)

3. Sponsor/Collaborators

Name of the Sponsor
Brooke Army Medical Center

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The administration of N-acetyl-cysteine (an anti-oxidant) for seven days along with observation will result in improved hearing and balance function in individuals who demonstrate these disorders after blast exposure when compared to a placebo medicine and observation at the seven day time point.
Detailed Description
5.0 RESEARCH PLAN: The goal of this study is to examine the use of one anti-oxidant, N acetylcysteine (NAC), in individuals who suffer blast injury and demonstrate early sequela of mTBI. Recent changes in war fighting and operational situations have changed the injury patterns that our troops face in all aspects of military operations. Mild traumatic brain injury (mTBI) is among the most common injuries seen in the current theater of operations. While other injury patterns have shown a decrease over the last twelve months, mTBI from blast exposure has continued to be seen at increasing levels. This may be due in part to the fact that research has shown the individuals may suffer mTBI secondary to blast injury from one significant exposure or from repeated low level exposure which is more common as individuals rotate back to the theatre of operations for second, third, and even forth tours of duty. The sequela of mTBI include balance disorders, hearing loss, and cognitive dysfunction. These disorders can present immediately after the injury or several weeks after the injury but tests of function can detect injury shortly after the injury. Evidence exists in laboratory work and in human studies that anti-oxidant medicine can reduce/eliminate the sequela of mTBI if administered within 8-24 hours of injury. 5.1 OBJECTIVES: A population and single-subject design, double blinded, placebo controlled study comparing the effectiveness of the observation and administration of the anti-oxidant NAC to placebo in individuals suffering the sequela of mTBI after a single or multiple blast exposures. 5.2 HYPOTHESIS: The administration of NAC for seven days along with observation will result in improved hearing and balance function in individuals who demonstrate these disorders after blast exposure when compared to a placebo medicine and observation at the seven day time point 5.3 SPECIFIC AIMS: To determine the frequency of hearing loss and balance disorders in those exposed to blast injury that have non-emergent or non-urgent medical or surgical disorders and display a pattern of injury consistent with mTBI. To determine the effectiveness of one week of anti-oxidant, N-acetylcysteine combined with observation, in the reduction of hearing loss and balance disorders one week after injury as compared to placebo medication and observation. To determine the effectiveness of one week of anti-oxidant, N-acetylcysteine combined with observation, in the reduction of hearing loss and balance disorders six months after injury as compared to one week of placebo medication and observation.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Mild Traumatic Brain Injury
Keywords
mild traumatic brain injury, anti-oxidant, early treatment

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
150 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
2
Arm Type
Placebo Comparator
Arm Description
control
Arm Title
1
Arm Type
Experimental
Arm Description
Active medicine
Intervention Type
Drug
Intervention Name(s)
N-acetyl-cysteine (NAC)
Intervention Description
Anti-oxidant in a pill format
Intervention Type
Drug
Intervention Name(s)
Placebo
Intervention Description
Control for study
Primary Outcome Measure Information:
Title
Relief of symptoms of mTBI
Time Frame
7 days

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
50 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Be active duty United States Service member Be between the ages of 18 and 50 years Present to TQ Surgical within 24 hours of blast exposure. Have complains consistent with possible TBI including hearing loss, dizziness, lightheadedness, cognitive difficulties, and/or had loss of consciousness. Are not expressly excluded by the criteria listed below. Exclusion Criteria: Require urgent or emergent surgical procedures. Will require medical evacuation to any level III or higher facility (other then to a level III for a CT scan only). Has evidence of an open head wound. Pregnant Females The use, within the last seven days, of a nutritional supplement containing an anti-oxidant.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Michael E. Hoffer, M.D.
Organizational Affiliation
U.S. Military
Official's Role
Principal Investigator
Facility Information:
Facility Name
TQ Surgical
City
AL Taqaddum
Country
Iraq

12. IPD Sharing Statement

Citations:
PubMed Identifier
23372680
Citation
Hoffer ME, Balaban C, Slade MD, Tsao JW, Hoffer B. Amelioration of acute sequelae of blast induced mild traumatic brain injury by N-acetyl cysteine: a double-blind, placebo controlled study. PLoS One. 2013;8(1):e54163. doi: 10.1371/journal.pone.0054163. Epub 2013 Jan 23.
Results Reference
derived

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The Use of Anti-oxidants to Reduce Sequela of Mild Traumatic Brain Injury (mTBI) After Blast Exposure

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