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Non-invasive Intracranial Pressure Monitoring in Brain Tumor Patients

T

Tanta University

Status

Not yet enrolling

Conditions

Intracranial Pressure Increase
Brain Neoplasm

Treatments

Diagnostic Test: Ocular Sonography

Study type

Observational

Funder types

Other

Identifiers

NCT07286396
ICP measurement

Details and patient eligibility

About

This research protocol focuses on the pre- and post-operative evaluation of ICP using non-invasive methods, particularly in the context of surgery for brain tumor removal. By utilizing ocular ultrasound to measure ONSD and ONSD/ETD ratios, this study hypothesizes that the utility of these parameters in monitoring ICP pre- and post-operative periods could be effective.

Full description

This research protocol focuses on the pre- and post-operative evaluation of ICP using non-invasive methods, particularly in the context of brain tumor resection surgery. By utilizing ocular ultrasound to measure ONSD and ONSD/ETD ratios, this study hypothesizes that the utility of these parameters in monitoring ICP pre- and post-operative periods could be effective.

This study aims to evaluate the effectiveness of the ONSD and the ONSD/ETD ratio using ultrasound as a non-invasive method for measuring intracranial pressure pre- and post-operatively in brain tumor patients.

Enrollment

60 estimated patients

Sex

All

Ages

21+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • • Adult patients (>21 years) undergoing brain tumor resection surgery.

    • Preoperative imaging-confirmed diagnosis of the tumor.
    • American Society of Anesthesiologists (ASA) physical status II to IV
    • Consent to participate in the study.

Exclusion criteria

  • • Preexisting ocular conditions affecting the optic nerve or globe integrity, such as glaucoma, thyroid-associated ophthalmopathy, or other optic nerve diseases.

    • Combined ocular and optic nerve injuries at admission.
    • History of cranial trauma, prior neurosurgery, or lumbar puncture performed within 2 weeks before the measurement of optic nerve sheath diameter (ONSD).
    • History of subarachnoid hemorrhage (SAH).
    • Serious complications that could affect life expectancy, such as hematological disorders or malignancies.
    • Refusal to participate or withdrawal of consent at any stage.

Trial contacts and locations

1

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Central trial contact

tarek AH Mostafa; sameh Ahmed

Data sourced from clinicaltrials.gov

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