- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00744003
An Observational Study of Early Coagulopathy, or Clotting Disorder, in Injured Patients
Early Trauma Induced Coagulopathy (ETIC): A Pilot Study to Determine Its Definition and Risk Factors
Study Overview
Status
Conditions
Study Type
Contacts and Locations
Study Locations
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Georgia
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Atlanta, Georgia, United States, 30303
- Grady Memorial Hospital
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- > 17 years of age
GMH Emergency Care Center (ECC) admission with trauma team activation - referred to by GMH nomenclature as a "STAT-pack." Trauma team activation criteria were developed from standard criteria published by the American College of Surgeons Committee on Trauma and published in Resources for Optimal Care of the Injured Patient manual 2006 edition and modified for GMH use. A trauma patient is declared a STAT-pack if they meet one of the following criteria:
- Ejection from a motor vehicle or motorcycle
- Extremes of age: pediatric < 6 years of age or an adult > 65 yrs of age
- One of the following: HR > 120; RR > 30; Systolic BP < 100; GCS < 13; Basal temperature < 35 degrees C
- Penetrating trauma to head/neck/thorax/abdomen including flank and back/antecubital fossa/groins/popliteal space
- Suspected neurological injury i.e. spinal cord injury
- Traumatic amputation above the wrist or ankle
- Mangled or crush to an extremity
- History of trauma in a patient who is combative, has deteriorating vital signs or is hemorrhaging from an open wound
- Physician or EMS discretion
- Patients admitted to GMH ECC directly from the site of injury
Exclusion Criteria:
- < 18 years of age
- Any patient who is pronounced dead by health care personnel prior to any blood sampling
- Any patient who arrives undergoing CPR and is pronounced dead without resumption of vital signs
- Transfers from other health care facilities
- Any patient known to be taking anti-coagulant or anti-platelet medicine
- Any patient with a known predisposing history of a coagulation or platelet defect
Study Plan
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Development of coagulopathy as defined by abnormal PT/INR
Time Frame: Admission to Trauma Center
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Admission to Trauma Center
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Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Jana BA MacLeod, MD, Assistant Professor Of Surgery, Emory University School of Medicine
Study record dates
Study Major Dates
Study Start
Primary Completion (ACTUAL)
Study Completion (ACTUAL)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (ESTIMATE)
Study Record Updates
Last Update Posted (ESTIMATE)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- IRB00006685
- ETIC Study (OTHER: Other)
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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