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Evaluation of Postoperative Intracranial Pressure in Patients Undergoing Intracranial Tumor Surgery

S

Sezen Kumaş Solak

Status

Not yet enrolling

Conditions

INTRACRANIAL PRESSURE
INTRACRANIAL TUMOR
OPTIC NERVE

Treatments

Procedure: USG
Procedure: BCT

Study type

Interventional

Funder types

Other

Identifiers

NCT06559566
BAGCILAR 3

Details and patient eligibility

About

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.

Full description

Optic Nerve Sheath Diameter (ONSD) Measurement is a non-invasive diagnostic method used to detect increased intracranial pressure, and in general, ONSD measurement over 5 mm has been found to be associated with increased intracranial pressure.ONSD will be measured using an USG device within the specified time periods.

T0: Before anesthesia induction T1: First 5 minutes immediately after induction of anesthesia T2: At the end of the surgery before extubation /minute T3: Within the first hour/minute after extubation T4: 12 hours/minute after tumor resection T5. 24 hours/minute after tumor resection

ONSD measurement in brain computer tomography (BCT); Eyeball diameter and optic nerve diameter measurements will be made on BCT transverse images at the optic nerve level and recorded.In patients, USG and BCT correlation comparison is planned before the operation (T0), in the first hour after the end of post-operative surgery (T3) and at the 24th hour after post-operative surgery (T5).

T0: ONSD measurement in pre-operative Brain CT T3: BCT ONSD measurement/minute within the first hour following the postoperative period T5: BCT ONSD measurement/minute 24 hours following the postoperative period

Enrollment

50 estimated patients

Sex

All

Ages

18 to 65 years old

Volunteers

No Healthy Volunteers

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)

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Triple Blind

50 participants in 2 patient groups

ONSD measurement with USG
Active Comparator group
Description:
After the ONSD measurement is made before anesthesia induction, general anesthesia will be given to each patient according to the institutional protocol. The ONSD measurements of the patients will be measured according to the T0, T1, T2, T3, T4, T5 time period by a person who has experience in using USG T0: Before anesthesia induction T1: First 5 minutes immediately after induction of anesthesia T2: At the end of the surgery before extubation /minute T3: Within the first hour/minute after extubation T4: 12 hours/minute after tumor resection T5. 24 hours/minute after tumor resection
Treatment:
Procedure: USG
ONSD measurement with BCT
Active Comparator group
Description:
In patients, USG and BCT correlation comparison is planned before the operation (T0), in the first hour after the end of post-operative surgery (T3) and at the 24th hour after post-operative surgery (T5). T0: ONSD measurement in pre-operative BCT T3: BCT ONSD measurement/minute within the first hour following the postoperative period T5: BCT ONSD measurement/minute 24 hours following the postoperative period The measurement of ONSD in BCT is; Eyeball diameter and optic nerve diameter measurements will be made on BCT transverse images at the optic nerve level and recorded.
Treatment:
Procedure: BCT

Trial contacts and locations

0

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Central trial contact

SEZEN KUMAS SOLAK, MD

Data sourced from clinicaltrials.gov

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