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Perioperative Evaluation of Intracranial Hypertension by Ultrasound Measurement of Variations in the Diameter of the Sheath of the Optic Nerve in the Excision of a Tumor or Biopsy Supratentorial Brain

P

Poitiers University Hospital

Status

Completed

Conditions

Supratentorial Brain Tumor

Treatments

Procedure: ultrasound measurement of variations in the diameter of the sheath of the optic nerve

Study type

Interventional

Funder types

Other

Identifiers

NCT01864499
DINO-NEURO

Details and patient eligibility

About

Neurosurgery for supratentorial brain tumor is frequently associated with preoperative intracranial hypertension. The evaluation of intracranial pressure is available noninvasively by measuring the diameter of the optic nerve sheath ultrasound.

The evaluation of intracranial pressure by measuring the DNO in perioperative is not described in the literature. The investigators propose a pilot study to assess intracranial pressure perioperative surgery for supratentorial brain tumor. The investigators consider a diameter of the optic nerve sheath as normal and predictive of intracranial pressure below 20 mm Hg when less than 5.7 mm (on the average of two measurements on each eye). DNO the normal healthy adult unanesthetized is 5 mm.

The main objective of the study is to compare the mean change in diameter of the optic nerve between the postoperative and D2 between groups of patients undergoing resection of a brain tumor and patients undergoing biopsy brain tumor.

Pilot Study: Prospective, single-center, controlled, non-randomized, the number of patients is estimated according to the recruiting capabilities of neurosurgery for this type of patient in the institution, A total of 40 patients: 20 patients Tumor Resection, control group: 20 patients Biopsy Brain Tumor.

Sex

All

Ages

18 to 99 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Age ≥ 18 years
  • Hospitalized for surgery of intracerebral tumors in the study group.
  • Hospitalized for a biopsy of intracerebral tumor lesion in the control group.

Exclusion criteria

  • Age <18 years
  • Enucleation Prohibited to the achievement of an ocular ultrasound
  • Hypersensitivity to gel
  • Eye Wound
  • Massive facial fracture
  • Skin Infection Site

Trial design

0 participants in 2 patient groups

Tumor Resection
Experimental group
Treatment:
Procedure: ultrasound measurement of variations in the diameter of the sheath of the optic nerve
Biopsy Brain Tumor
Active Comparator group
Treatment:
Procedure: ultrasound measurement of variations in the diameter of the sheath of the optic nerve

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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