Efficacy and Safety of Baricitinib in the Post-intracerebral Hemorrhage Pulmonary Injury

Recruiting Phase 1 Phase 2 Interventional Study
Pulmonary Injury After Intracerebral Hemorrhage
No Placebo Group Every participant receives an active treatment — no one gets a placebo. Prior Safety Data This treatment has already been tested in at least one earlier human trial.
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At a Glance
Age
18 and older
Sex
Any
Trial phase
Phase 1/2
Study type
Interventional
Purpose
Basic Science
Participants needed
100 (estimated)
Sponsor
Tianjin Medical University General Hospital · Other
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About This Trial
Some patients with intracerebral hemorrhage will develop severe lung injury such as respiratory distress syndrome. Baricitinib has been approved by the FDA for severe pneumonia caused by the coronavirus, and has been used in the treatment of hospitalized patients with COVID-19. Baricitinib significantly reduced the risk of death and shortened the length of stay in COVID-19 patients. According to c…
Trial Locations
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Eligibility Criteria
Inclusion Criteria: 1. Male or female patients ≥ 18 years old; 2. The diagnosis was non-traumatic intracerebral hemorrhage, subarachnoid hemorrhage (including supratentorial deep hemorrhage, lobal hemorrhage, cerebellar hemorrhage, brainstem hemorrhage, intracerebral hemorrhage, intracerebral paren…
Contacts

Qiang Liu, M.D, Ph.D.

+86 15022439149

qliu@tmu.edu.cn

CONTACT