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Clinical Trials/NCT03666949
NCT03666949UnknownNot Applicable

NEURANESTH General Anesthesia Versus Locoregional Anesthesia for Evacuation of Chronic Subdural Hematomas: A Prospective Randomized Trial

University Hospital, Caen1 site in 1 country60 target enrollmentStarted: May 1, 2018Last updated:
Conditions
Interventions
Drugs

Trial Snapshot

Phase
Not Applicable
Enrollment
60
Locations
1
Primary Endpoint
postoperative theoretical length of stay

Study Overview

Brief Summary

This study compare general anesthesia versus locoregional anesthesia for evacuation of chronic subdural hematoma. Half of participant will be operated under general anesthesia, while the other half will be operated under locoregional anesthesia.

Detailed Description

General anesthesia is the most common technique for this surgery. The local anesthesia is less common but it allows to obtain the same surgical result. This last technique being more recent little study compared these two techniques in terms of complications and postoperative consequences.

The investigators will randomize patients into two groups (a general anesthesia group and a locoregional anesthesia group).

General anesthesia provides complete immobility and optimal surgical comfort but is a source of multiple complications, especially in a population of polypathological and polymedicated elderly patients (which is the population affected by chronic subdural hematomas).

Locoregional anesthesia requires special technical training, leads to complete analgesia of the surgical procedure but does not involve complete immobility of the patient, however this technique probably leads to less postoperative complications and allows a more early rehabilitation.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
None

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • subdural chronic hematoma uni or bilateral
  • Obtaining an oral consent
  • french speaker
  • affilliation to French social security

Exclusion Criteria

  • Patients agitated or not cooperating, not allowing the realization of a locoregional anesthesia
  • Patients with other intracranial lesions
  • Patients with underlying neurological pathology with a modified Rankin score greater than 1
  • Pregnant or lactating women
  • Patients under guardianship / curatorship

Arms & Interventions

All General anesthesia

Other

Use of a hypnotic("propofol 2.5mg/kg"), morphine("remifentanil1yg/kg") and curare("atracurium0.5mg/kg"), with the support of orotracheal intubation and mechanical ventilation

Intervention: All General anesthesia (Drug)

All Locoregional anesthesia

Other

Use of a local anesthetic(" xylocaine 1%") for the realization of scalp nerve block

Intervention: All Locoregional anesthesia (Drug)

Outcomes

Primary Outcomes

postoperative theoretical length of stay

Time Frame: 10 days

Theoretical duration of postoperative hospitalization: discharge authorized after medical checklist

Secondary Outcomes

  • MINI COG: Measurement of postoperative cognitive impairment at 6 months(2 days)
  • Modified Rankin score (0-6)(3 month)
  • LIKERT scale: a measure of the degree of satisfaction of the surgeon and the patient.(baseline)
  • Rates of postoperative surgical complications(10 days)
  • Postoperative medical complications rate(10 days)
  • Mortality rate at 6 months.(6 month)
  • Simple numeric scale for postoperative pain(2 days)
  • Opioid consumption(10 days)
  • Admission rate in Intensive care unit(3 month)

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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