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OpenTrials
Completed

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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Key information

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

intraventricual recombinant tissue plasminogen activator application

Drug

Primary outcomes

  1. 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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