Status:

COMPLETED

Dexmedetomidine Versus Propofol for Sedation in Stereotactic Brain Biopsy

Lead Sponsor:

Ain Shams University

Conditions:

Adverse Effects in the Therapeutic Use of Other and Unspecified Agents Primarily Acting on the Respiratory System

Eligibility:

All Genders

20-60 years

Phase:

PHASE4

Brief Summary

Pre-operative anxiety leads to higher sympathetic stimulation. Propofol in the main drug used during interventional or imaging techniques that need sedation. Also, dexmedetomidine causes sedation, ana...

Eligibility Criteria

Inclusion

  • Inclusion criteria:
  • Patients with:
  • brain secondaries from the lung/breast/pancreas
  • tuberculoma
  • pyogenic abscess
  • intra-axial supratentorial space occupying lesion with or without hydrocephalus \*an average duration of the procedure 1- 2hr 30 min
  • an available caregiver for overnight observation
  • patient relative proximity to the hospital Exclusion criteria
  • Patients with:
  • morbid obesity (body mass index \>35 kg/m2)
  • significant comorbidities (a known history of hepatic disease, renal dysfunction, hypertension, and chronic pain)
  • history of drug or alcohol abuse
  • an allergic reaction to one of the study medications
  • anticipated difficult airway
  • uncontrolled epilepsy
  • poor neurological status
  • neuropsychological unsuitability taking psychotropic drugs (benzodiazepines and barbiturates)
  • patients with brain stem lesions (vital areas of brain)
  • un-cooperative
  • refusing adults
  • patients with ventricular drain
  • already inpatient
  • Intubated patients and those who had a prior craniotomy .

Exclusion

    Key Trial Info

    Start Date :

    September 1 2016

    Trial Type :

    INTERVENTIONAL

    Allocation :

    ACTUAL

    End Date :

    December 1 2017

    Estimated Enrollment :

    60 Patients enrolled

    Trial Details

    Trial ID

    NCT03375385

    Start Date

    September 1 2016

    End Date

    December 1 2017

    Last Update

    April 1 2022

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