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Clinical Application of Low-Field Magnetic Resonance Imaging in Patients on Extracorporeal Cardiopulmonary Resuscitation

Clinical Application of Low-Field Magnetic Resonance Imaging in Patients on Extracorporeal Cardiopulmonary Resuscitation

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07526701
Enrollment
36
Registered
2026-04-13
Start date
2024-11-01
Completion date
2026-01-01
Last updated
2026-04-13

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

Conditions

Acute Brain Injury, Cardiac Arrest (CA), Extracorporeal Cardiopulmonary Resuscitation

Keywords

Cardiac Arrest, Extracorporeal Cardiopulmonary Resuscitation, Acute brain injury, Magnetic Resonance Imaging

Brief summary

Timely identification of acute brain injury (ABI) patterns in patients with extracorporeal cardiopulmonary resuscitation (ECPR) is essential for prognostic assessment and optimization of clinical management, particularly anticoagulation strategies. This study aimed to evaluate the safety and feasibility of early 0.23-T MRI examination in ECPR patients. The investigators further assessed the image quality of the 0.23-T MRI and investigated the incidence and patterns of ABI, as well as their associations with neurological outcomes. This prospective observational study was conducted in the emergency intensive care unit (EICU) of Beijing Chaoyang Hospital, a high-volume ECPR center. The primary outcome was the feasibility of performing 0.23-T MRI in patients undergoing ECPR, defined as successful completion of the examination without serious adverse events (AEs).

Interventions

None listed

Sponsors

Capital Medical University
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 75 Years
Healthy volunteers
No

Inclusion criteria

* Enrolled patients were those with out-of-hospital cardiac arrest of presumed cardiac cause, supported by ECPR, who achieved ROSC but remained unconscious and unable to obey verbal commands.

Exclusion criteria

* age \< 18 years * unwitnessed cardiac arrest * pregnancy * contraindications to MRI (except ECPR, for which safety with 0.23-T MRI has been proved) * physical dimensions exceeding scanner limits * refusal of consent by the family

Design outcomes

Primary

MeasureTime frameDescription
Feasibility of 0.23-T MRI examinationFrom the initiation of the MRI scan until 6 hours after its completion.Defined as the percentage of participants who successfully complete the MRI examination without experiencing serious adverse events (AEs). AEs include a decrease in ECMO flow \> 10%, a change in mean arterial pressure of ± 20%, or a change in minute ventilation \> 20%.

Secondary

MeasureTime frameDescription
Image QualityWithin 6 hours after the completion of the MRI scan.Assessment of the diagnostic quality of 0.23-T MRI images by board-certified neuroradiologists to evaluate noise, artifacts, and anatomical clarity.
Incidence of Acute Brain Injury (ABI)From the onset of cardiac arrest to the completion of the MRI scanThe proportion of patients identified with ABI patterns (such as ischemic stroke, intracranial hemorrhage, or cerebral edema) based on 0.23-T MRI findings.
The association between ABI and neurological outcomes3 months after ROSC.Neurological outcomes were assessed at 3 months after ROSC using the Glasgow-Pittsburgh Cerebral Performance Category (CPC) scale. The CPC scale ranges from 1 to 5, with 1 indicating good performance, 2 indicating moderate disability, 3 indicating severe disability, 4 indicating vegetative state and 5 indicating brain death or death. The neurological outcomes were categorized as favorable prognosis (CPC 1-2) and poor prognosis (CPC 3-5).

Countries

China

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Apr 14, 2026