Dysregulated CNS Inflammation After Acute Brain Injury
Completed
Conditions studied: Traumatic Brain Injury, Aneurysmal Subarachnoid Hemorrhage
In brief
By doing this study, the investigator hopes to learn how the levels of important proteins involved in inflammation change over time in patients with acute brain injury. The total amount of time participants will be asked to volunteer for this study is approximately two hours over a five day period.
Key facts
- Study ID
- NCT03287557
- Run by
- University of Kentucky
- People needed
- 8
- Starts
- 2018-01-02
- Expected to finish
- 2019-05-24
- Last updated by the study team
- 2019-08-29
Who can join
Age: 18 and older, up to 101. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- severe, non-penetrating TBI or aSAH
- must have a ventriculostomy (EVD) placed by the UK Neurosurgery service within 12 hours of primary traumatic episode
You may not qualify if…
- non-survivable brain injury or other organ system injury
- life expectancy is five days or less
- penetrating TBI
- status epilepticus upon arrival to the hospital
- severe ischemic heart disease or congestive heart failure, myocardial infarction, or spinal cord injury
- Takotsubo cardiomyopathy secondary to the SAH
- active cancer or have been treated for cancer within the previous 6 months
Where it is running
- University of Kentucky Deparment of Neurosurgery, UK Chandler Hospital — Lexington, Kentucky, United States
Full record on ClinicalTrials.gov
Trial information comes from ClinicalTrials.gov and is refreshed daily. TrialsForMe does not provide medical care and does not run the studies it lists.