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Clinical Trials in Italy / NCT07580326
Active, not recruiting Observational

Microplastics in Brain Hematomas and Neurological Outcomes After Intracerebral Hemorrhage

NCT07580326 · tracked via the Priya Life Science Italy tracker
Phase
Observational
Started
2024-06-01
Last updated
2026-06-02

Condition(s) studied

Intracerebral HemorrhageBrain Hematoma

Investigational drug(s) / intervention(s)

Observational Analysis

Observational Analysis: No intervention is administered as part of the study. All patients receive standard clinical care according to current guidelines for intracerebral hemorrhage. Biological samples, including intracerebral hematoma tissue and peripheral blood, are collected for observational analysis of micro- and nanoplastics and their association with clinical, radiological, and biological outcomes.

Study summary

This observational study investigates the presence of micro- and nanoplastics in surgically removed intracerebral hematomas and their association with neurological outcomes in patients with spontaneous intracerebral hemorrhage.

Microplastics have recently been identified in human tissues and are increasingly recognized as potential contributors to inflammation and vascular dysfunction. However, their role in cerebrovascular diseases, particularly intracerebral hemorrhage, remains unknown.

Patients undergoing surgical hematoma evacuation will be enrolled. Brain tissue and blood samples will be analyzed using advanced spectroscopic and imaging techniques to detect and characterize micro- and nanoplastics.

The study aims to evaluate whether the presence of these particles is associated with increased inflammation, worse neurological outcomes, and higher risk of adverse cerebrovascular events.

This research may provide novel insights into the impact of environmental pollutants on brain vascular disease and patient prognosis.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Age ≥18 years * Diagnosis of spontaneous intracerebral hemorrhage confirmed by CT or MRI * Indication for surgical hematoma evacuation * Availability of intracerebral hematoma tissue sample * Ability to provide informed consent (patient or legal representative) Exclusion Criteria: * Traumatic intracerebral hemorrhage * Intracranial neoplasms * Known vascular malformations (e.g., arteriovenous malformations, aneurysms) * Severe systemic infection or sepsis at admission * Inadequate or contaminated biological samples * Refusal or inability to provide informed consent

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
University Hospital Luigi Vanvitelli Naples Italy

More University of Campania Luigi Vanvitelli trials in Italy

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07580326 on ClinicalTrials.gov ↗ ← All trials in Italy