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N/A N=36 Single-blind Other

Sedatives' Effects on Neurological Function in Patients With Eloquent Area Glioma

Glioma

Enrolled (actual)
36
Serious AEs
0.0%
Results posted
Aug 2017
Primary outcome: Primary: Task Completing Time Change Between Sedation and Baseline Measured by 9-hole Peg Test — 27.8; 19.1; 54.3; 21.4 seconds — p=<0.01

Study Design & Population

Study type
Interventional
Phase
N/A
Interventions
Midazolam (Drug)
Age
Adult · 18+ yrs
Sex
All
Sponsor
Beijing Tiantan Hospital
Primary completion
Mar 2017

Outcome Measures

OutcomeResultp-value
PRIMARY
Task Completing Time Change Between Sedation and Baseline Measured by 9-hole Peg Test
27.8; 19.1; 54.3; 21.4; 21.8; 19.1 <0.01 sig
SECONDARY
Number of Participants With OAA/S=4 After Sedation
15; 17
SECONDARY
Mean Arterial Blood Pressure (MAP) as a Measure of Physiological Change
96.5; 95.7; 96.2; 91.2; 95.4; 88.2
SECONDARY
Heart Rate as a Measure of Physiological Change
78.1; 79.0; 84.3; 79.0; 81.5; 71.5
SECONDARY
Brain Glioma Pathological Diagnose as a Measure of Tumor Type
6; 9

Summary

Sedation in the operating room, the Post Anesthesia Care Unit and the Intensive Care Unit is common and often necessary for patients with intracranial brain tumor. Repeated neurological function assessments is needed in those locations, especially in patients with tumors in or near eloquent regions, this is to monitor their neurologic performance to determine if there are alterations that require treatment. Some slowly infiltrative low-grade gliomas near eloquent regions do not show any detectable neurologic deficits, perhaps from reorganization, but with sedation by some sedatives such as benzodiazepine midazolam and anesthetic hypnotic propofol, the disease may seem much worse resulting in inappropriately aggressive treatment. This may be especially problematic in patients undergoing awake craniotomy for tumors in eloquent regions. This is a single-center perspective study. Patients will be mildly sedated to keep them responsive and cooperative. Motor and sensory function will be evaluated before and after mild sedation. Specific benzodiazepine antagonist will be used if sedated by midazolam. The purpose of this study is to observe if commonly used benzodiazepine midazolam exacerbates or unmasks motor and sensory function in patients with intracranial eloquent area gliomas. Hypothesis: mild sedation can unmasks or exacerbate motor and sensory deficits in patients with eloquent area glioma but not in non-neurosurgical patients/healthy volunteers. If the neurologic deficits induced by benzodiazepine agonist, then can be reversed by flumazenil.

Eligibility Criteria

Inclusion Criteria

  • Age between 18-60 year-old
  • American Society of Anesthesiology(ASA) status I~II
  • Elective craniotomy patients with supratentorial eloquent glioma diagnosed by MRI (In control group: volunteers without neuro-diseases)

Exclusion Criteria

  • Unable to comprehend and cooperate with the neurologic examination
  • Impaired mental status
  • Taking sedative drugs in the past 24 hours
  • Taking pain reliever in the past 24 hours
  • Drug and/or alcohol abuse
  • Pregnant and/o lactating women
  • Recurrent brain tumors
  • Multiple brain tumors
  • Accepting radiotherapy or chemotherapy
  • Complicated with intracranial trauma and vascular diseases
  • Complicated with grand mal epilepsy ( in midazolam group)
  • Complicated with neuromuscular diseases
  • Complicated with cutaneous paresthesia
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT02439164). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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