Not Yet RecruitingNot Applicable

Evaluation of Postoperative Intracranial Pressure in Patients Undergoing Intracranial Tumor Surgery

50 participantsStarted 2024-09-15

Plain-language summary

Ultrasonography(USG)-guided optic nerve sheath diameter measurement and its correlation with brain computed tomography in the evaluation of intracranial pressure in patients who underwent intracranial brain tumor surgery.

Who can participate

Age range

18 Years – 65 Years

Sex

ALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * Patients over 18 -65 years * Brain malignant neoplasm tumor * Brain benign neoplasm supratentorial * Brain benign neoplasm infratentorial information Exclusion Criteria: * Patients who cannot provide adequate image quality in ocular ultrasonography * Who are unconscious or have a Glasgow coma scale of less than 15 * Pseudotumor cerebri * Optic nerve arachnoid cyst * Patients with open injuries involving the eyelid and surrounding area * Optic nerve malignant neoplasm * Injury of the optic nerve and its pathways * Systemic Lupus Erythematosis, * Scleroderma * Multiple Sclerosis, sarcoidosis * Thyrotoxicosis (hyperthyroidism)

Questions worth asking your doctor

Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.

1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?

Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.

Questions for the trial coordinator

The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.

1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?

A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.

What they're measuring

intracranial pressure

Timeframe: T0: Before anesthesia induction T1: peroperative5. minutes T2: At the end of the surgery 6.hours T3:after extubation 1 hours T4: postoperative 12.hours T5. postoperative 24.hours

Trial details

NCT IDNCT06559566

SponsorSezen Kumaş Solak

Sponsor typeOTHER_GOV

Study typeINTERVENTIONAL

Primary completion2025-02-01

Contact for this trial

SEZEN KUMAS SOLAK, MD

+905055729494 sezenkumassolak@gmail.com

View on ClinicalTrials.gov More INTRACRANIAL TUMOR trials

Who can participate

Age range

18 Years – 65 Years

Sex

ALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.