Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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RECRUITING
24 participants
OBSERVATIONAL
2024-12-01
2027-09-30
Brief Summary
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Abnormal accumulation of hyaluronic acid in the lungs has been reported to be closely related to the pathological progression of various pulmonary injury diseases, such as chest trauma, pulmonary infection and chronic obstructive pulmonary disease. From this, the present research is aimed to explore the levels and dynamic changes of hyaluronic acid in the bronchoalveolar lavage fluid and blood of patients with acute lung injury following SAH, and to analyze its correlation with the prognosis of pulmonary complications, thereby providing assistance for the clinical diagnosis and treatment of SAH.
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Detailed Description
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Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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Subarachnoid Hemorrhage (SAH)
No interventions assigned to this group
Eligibility Criteria
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Inclusion Criteria
* A documented diagnosis of SAH within 5 days.
* A Hunt-Hess scale of Ⅳ or Ⅴ.
* Absence of clinical and etiological evidence of pulmonary infection.
Exclusion Criteria
* Present history of traumatic brain injury or intracranial hemorrhage.
* Past history of neurological disorders, lung infection within the past six months, cancer, chronic cardiopulmonary diseases, hematological diseases or renal failure.
* Have participated in clinical trials in the past 4 weeks.
* The investigator considers that not appropriate for inclusion.
18 Years
80 Years
ALL
No
Sponsors
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Tianjin Medical University
OTHER
Responsible Party
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Xintong Ge
Director
Principal Investigators
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Xintong Ge
Role: STUDY_CHAIR
Tianjin Medical University General Hospital
Yadan Li
Role: PRINCIPAL_INVESTIGATOR
Tianjin Huanhu Hospital
Ye Tian
Role: PRINCIPAL_INVESTIGATOR
Tianjin Medical University General Hospital
Locations
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Tianjin Medical University General Hospital
Tianjin, , China
Countries
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Central Contacts
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Facility Contacts
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Provided Documents
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Document Type: Study Protocol, Statistical Analysis Plan, and Informed Consent Form
Other Identifiers
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IRB2024-YS-425-01
Identifier Type: -
Identifier Source: org_study_id
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