ALI & Pulmonary HA Deposition After SAH

NCT ID: NCT06628531

Last Updated: 2025-11-19

Study Results

Results pending

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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Recruitment Status

RECRUITING

Total Enrollment

24 participants

Study Classification

OBSERVATIONAL

Study Start Date

2024-12-01

Study Completion Date

2027-09-30

Brief Summary

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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.

Detailed Description

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Conditions

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Subarachnoid Haemorrhage (SAH)

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

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Subarachnoid Hemorrhage (SAH)

No interventions assigned to this group

Eligibility Criteria

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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.
Minimum Eligible Age

18 Years

Maximum Eligible Age

80 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Tianjin Medical University

OTHER

Sponsor Role lead

Responsible Party

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Xintong Ge

Director

Responsibility Role PRINCIPAL_INVESTIGATOR

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

Site Status RECRUITING

Countries

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China

Central Contacts

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Xintong Dr. Ge

Role: CONTACT

86-13662055012

Facility Contacts

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Yi Wang

Role: primary

86-022-60362237

Provided Documents

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Document Type: Study Protocol, Statistical Analysis Plan, and Informed Consent Form

View Document

Other Identifiers

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IRB2024-YS-425-01

Identifier Type: -

Identifier Source: org_study_id

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