NCT Number: NCT03452722
Neuroinflammatory Response in Patients With ICH and IVH Treated With rtPA
This study compares the neuroinflammatory response in patients with hypertensive ICH associated with IVH treated with intraventriculary applied rtPA, and the control group. The inflammatory mediator concentration is analyzed in local cerebrospinal liquor.
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Notify MeKey information
Conditions
Age range
18 year–80 year
Sex eligibility
All sexes
Study type
Observational
Who can participate
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
- Subjects with primary ICH with IVH
- ICH score 2-4, , with origin of the hematoma in the basal ganglia and blood in the third and/or ventricle
- Patient is not considered a surgical candidate by neurosurgery service
Exclusion criteria
- No history of diseases or drugs that affect the immunological system.
- ICH score 1 and 5
- Current participation in another research drug treatment protocol
- Previously known intracranial arteriovenous malformation or aneurysms
- Intracerebral hematoma considered to be related to trauma
- ICH is located in the pons
- Blood in the subarachnoid space visualized on CT scan
Treatment and study plan
Primary outcomes
-
Cytokine concentration difference between two groups
Time frame: Samples taken on day 0, day 1, day 3 and day 7.
Cytokine concentration measured from CSL
Sponsors and collaborators
Lead sponsor
University of Rijeka
Other
Registry information
Important dates
- Study start
- 2011
- Primary completion
- 2017
- Study completion
- 2018
- First posted
- Mar 2, 2018
- Registry last updated
- Mar 26, 2019
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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