Sign in

NCT07286396Not yet recruiting

Non-invasive Intracranial Pressure Monitoring in Brain Tumor Patients

Non-invasive Intracranial Pressure Monitoring in Brain Tumor Patients: A Prospective Observational Study of Optic Nerve Sheath Diameter Dynamics

Source: ClinicalTrials.gov · Last updated 16 Dec 2025

Brief summary (registry, in English)

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.

Status (registry)
Not yet recruiting
Study type
Observational
Enrollment
60 (estimated)
First submitted
2 Dec 2025
Start date
1 Jan 2026
Primary completion date
31 Dec 2026
Lead sponsor
Tanta University
NCT number
NCT07286396

What you commit to

  • Study type: Observational
  • Planned participants: 60
  • From 1 Jan 2026 to the primary completion date, 31 Dec 2026
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • • 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.

Who the study is looking for

  • • 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.

Age in the registry: 21 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Faculty of Medicine, Tanta University
Coordinator of this site? Confirm its status
TantaEgyptUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.