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Evaluation of Postoperative Intracranial Pressure in Patients Undergoing Intracranial Tumor Surgery

ConditionsINTRACRANIAL TUMORINTRACRANIAL PRESSUREOPTIC NERVE
Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-65
SponsorSezen Kumaş Solak

About this trial

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.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Patients over 18 -65 years

Brain malignant neoplasm tumor

Brain benign neoplasm supratentorial

Brain benign neoplasm infratentorial information

Disqualifiers

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

Trial design

Design model

Parallel

Treatments tested in this trial

  • USG

    Procedure/Surgery

    The aim of this study is to measure the intracranial pressure of patients planned for brain tumor surgery by measuring the optic nerve sheath diameter (ONSD) under USG guidance and compare its correlation with the computed brain tomography.

  • BCT

    Procedure/Surgery

    The aim of this study is to measure the intracranial pressure of patients planned for brain tumor surgery by measuring the optic nerve sheath diameter (ONSD) under USG guidance and compare its correlation with the computed brain tomography.

Treatment groups

50 Participants
are divided into 2 treatment groups
Group A: ONSD measurement with USGActive comparator 1 intervention
Group B: ONSD measurement with BCTActive comparator 1 intervention

Trial outcomes

Primary outcomes

1

intracranial pressure

To compare the optic nerve diameter measurement ,USG and BBT values used to measure intracranial pressure in patients with brain tumor surgery

Time frame
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

Secondary outcomes

1

Heart Rate

To compare the heart rate measurement

Time frame
T0: Before anesthesia induction T1: preoperative 5.minutes T2: At the end of the surgery 6.hoursT3:after extubation 1 hours T4: postoperative 12.hours T5. postoperative 24.hours
2

Blood pressure

To compare the blood pressure measurement

Time frame
T0: Before anesthesia induction T1: preoperative 5.minutes T2: At the end of the surgery 6.hours T3 extubation 1 hours T4: postoperative 12.hours T5. postoperative 24.hours

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

Sezen Kumaş Solak

Lead sponsor

Bagcilar Training and Research Hospital

Sponsor institution

Bagcilar Training and Research Hospital

Collaborator

Source ClinicalTrials.gov

This trial is not recruiting at the moment. You can still explore other options: