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ALI & Pulmonary HA Deposition After SAH

Relationship Between Acute Lung Injury and Pulmonary Hyaluronic Acid Deposition After Subarachnoid Hemorrhage

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06628531
Enrollment
24
Registered
2024-10-08
Start date
2024-12-01
Completion date
2026-09-30
Last updated
2026-03-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Subarachnoid Haemorrhage (SAH)

Keywords

Subarachnoid haemorrhage, SAH, acute lung injury, ALI, hyaluronic acid

Brief summary

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.

Interventions

None listed

Sponsors

Tianjin Medical University
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

* 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 Ⅳ or Ⅴ. * Absence of clinical and etiological evidence of pulmonary infection.

Exclusion criteria

* 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.

Design outcomes

Primary

MeasureTime frameDescription
Hyaluronic acid level in bronchoalveolar lavage fluid after SAHDuring the acute phase (1-5 days post-onset) and the chronic phase (10-14 days post-onset) of patients with SAHHyaluronic acid level (ng/ml) in bronchoalveolar lavage fluid at the acute phase (1-5 days post-onset) and the chronic phase (10-14 days post-onset) of patients with SAH
Inflammatory cytokines levels in bronchoalveolar lavage fluid after SAHDuring the acute phase (1-5 days post-onset) and the chronic phase (10-14 days post-onset) of patients with SAHInflammatory cytokines (IL-1β, TNF-α and IL-10) levels (pg/ml) in bronchoalveolar lavage fluid at the acute phase (1-5 days post-onset) and the chronic phase (10-14 days post-onset) of patients with SAH

Secondary

MeasureTime frameDescription
Serum hyaluronic acid level after SAHDuring the acute phase (1-5 days post-onset) and the chronic phase (10-14 days post-onset) of patients with SAHSerum hyaluronic acid level (ng/ml) at the acute phase (1-5 days post-onset) and the chronic phase (10-14 days post-onset) of patients with SAH
Serum inflammatory cytokines levels after SAHDuring the acute phase (1-5 days post-onset) and the chronic phase (10-14 days post-onset) of patients with SAHSerum inflammatory cytokines (IL-1β, TNF-α and IL-10) levels (pg/ml) at the acute phase (1-5 days post-onset) and the chronic phase (10-14 days post-onset) of patients with SAH

Countries

China

Contacts

CONTACTXintong Dr. Ge
xge@tmu.edu.cn86-13662055012
STUDY_CHAIRXintong Ge

Tianjin Medical University General Hospital

PRINCIPAL_INVESTIGATORYadan Li

Tianjin Huanhu Hospital

PRINCIPAL_INVESTIGATORYe Tian

Tianjin Medical University General Hospital

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 19, 2026