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Evaluating the Use of Thromboelastography to Diagnose Coagulopathy After Traumatic Brain Injury

The recruitment status of this study is unknown. The completion date has passed and the status has not been verified in more than two years.
Verified May 2015 by David K. Shellington, MD, University of California, San Diego.
Recruitment status was:  Recruiting
Sponsor:
ClinicalTrials.gov Identifier:
NCT01589172
First Posted: May 1, 2012
Last Update Posted: May 29, 2015
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Information provided by (Responsible Party):
David K. Shellington, MD, University of California, San Diego
April 27, 2012
May 1, 2012
May 29, 2015
May 2012
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Complete list of historical versions of study NCT01589172 on ClinicalTrials.gov Archive Site
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Evaluating the Use of Thromboelastography to Diagnose Coagulopathy After Traumatic Brain Injury
Evaluating the Use of Thromboelastography to Diagnose and Monitor Coagulopathy Associated With Pediatric Traumatic Brain Injury
The investigators will obtain thromboelastography (TEG) on pediatric patients admitted to the Rady Children's Hospital ICU after traumatic brain injury on admission to our ICU and after 24 hours of care. The investigators hypothesize that TEG will identify abnormalities of coagulation that are not identified by traditional coagulation studies, i.e. prothrombin time (PT), activated partial thromboplastin time (aPTT), and international normalized ratio (INR).
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Observational
Observational Model: Cohort
Time Perspective: Prospective
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Non-Probability Sample
Trauma patients admitted to the Rady Children's Hospital Pediatric Intensivse Care Unit
  • Traumatic Brain Injury
  • Coagulation Disorder
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Pediatric Brain Trauma Patients
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*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Unknown status
40
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Inclusion Criteria:

  • less than 15 years of age
  • evidence of intracranial bleed on CT scan or GCS <12

Exclusion Criteria:

  • No intracranial hemorrhage or
  • GCS 13 - 15
Sexes Eligible for Study: All
up to 15 Years   (Child)
No
Contact information is only displayed when the study is recruiting subjects
United States
 
 
NCT01589172
120296
No
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David K. Shellington, MD, University of California, San Diego
University of California, San Diego
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Principal Investigator: David K Shellington, MD University of California, San Diego
University of California, San Diego
May 2015