Actively Recruiting

Age: 18Years - 80Years
All Genders
NCT06628531

ALI & Pulmonary HA Deposition After SAH

Led by Tianjin Medical University · Updated on 2026-03-18

24

Participants Needed

1

Research Sites

95 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Acute lung injury is a common complication of subarachnoid hematoma (SAH), and a significant risk factor for death in patients with SAH. Unlike neurogenic pulmonary edema and pneumonia following brain injury, the clinical causes of pulmonary injury after SAH are not intracranial hypertension or pulmonary infection. Its occurrence is influenced by the release of catecholamines, the regulatory function of the hypothalamic-pituitary-adrenal (HPA) axis and systemic inflammatory response, but the specific mechanisms are still unclear. Therefore, delving into the pathological mechanisms of SAH-induced lung injury and developing therapeutic strategies based on the findings is of great importance to improve the prognosis of patients. 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.

CONDITIONS

Official Title

ALI & Pulmonary HA Deposition After SAH

Who Can Participate

Age: 18Years - 80Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age between 18 and 80 years old with independent behavior ability or authorized legal representative.
  • A documented diagnosis of SAH within 5 days.
  • A Hunt-Hess scale of III or IV.
  • Absence of clinical and etiological evidence of pulmonary infection.
Not Eligible

You will not qualify if you...

  • Pregnant or lactating women.
  • 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.

AI-Screening

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Trial Site Locations

Total: 1 location

1

Tianjin Medical University General Hospital

Tianjin, China, 300052

Actively Recruiting

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Research Team

X

Xintong Dr. Ge

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

1

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