Phase
Condition
Traumatic Brain Injury
Memory Loss
Neurologic Disorders
Treatment
N/AClinical Study ID
Ages 18-60 All Genders
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
Clinical diagnosis of TBI and a GCS 7-12
Only isolated TBI
CT
Pre-Trauma Karnofsky-Index = 100
Age 18-60 years
Male and female patients
Time to needle for study medication within 6 hours after injury
Patient is not pregnant or lactating during the trial and is not of childbearingpotential
Patient was able to speak, read and write in a pre-defined study language before theaccident.
Reasonable expectation of completion of outcome measures at follow-up
Written informed consent
Exclusion
Exclusion Criteria:
Evidence of pre-existing major health problems
Any neurological or non-neurological condition independent from TBI that mightinfluence the functional outcome or other efficacy outcome measures
Injury of writing hand influencing cognitive or other outcome measures
Clear clinical signs of intoxication influencing the evaluation
Major drug dependency including alcohol
Chronic treatment with steroids, Ca2+-channel blockers or major anticoagulants
Penetrating high-velocity missile head trauma
Stab wound trauma into the brain
Patients with spinal cord injury
Study Design
Connect with a study center
Prince of Wales Hospital
Hong Kong,
Hong KongSite Not Available
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