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Clinical Trials/NCT06903598
NCT06903598CompletedNot Applicable

Anesthesia and Analgesia Methods in Pediatric External Ventricular Drainage Placement

Hande Gurbuz1 site in 1 country63 target enrollmentStarted: August 25, 2021Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Sponsor
Enrollment
63
Locations
1
Primary Endpoint
Anesthesia method

Study Overview

Brief Summary

External ventricular drainage (EVD) provides cerebrospinal fluid drainage in hydrocephalus. In adults, the neurosurgeon can place EVD at the bedside. In children, it is mainly preferred to be placed in the operating room under general anesthesia. However, general anesthesia may negatively affect oxygenation (during the intubation period) or cerebral blood flow (due to hypotension). This study investigates the use of regional block methods (without general anesthesia) in children for EVD placement.

Detailed Description

External ventricular drainage (EVD) provides cerebrospinal fluid drainage in hydrocephalus. In adults, EVD can be placed by the neurosurgeon at the bedside. In children, it is mainly preferred to be placed in the operating room under general anesthesia. However, general anesthesia may negatively affect oxygenation during a prolonged intubation period, leading to hypoxemia. Furthermore, hypotensive effects of general anesthesia may cause ischemia due to decreased cerebral blood flow.

Additionally, on the other hand, painful stimuli caused by surgical incisions or pins may cause hemorrhagic events due to a hypertensive period. Therefore, scalp blocks and local anesthetic infiltrations are recommended to prevent such adverse events. Although general anesthesia has been a routine for many anesthesiologists for EVD placement in children, this research hypothesizes that scalp blocks (along with sedatives) can be used as an anesthesia method for EVD placement.

This study investigates the use of regional block methods (to avoid general anesthesia) in children for EVD placement.

Study Design

Study Type
Observational
Observational Model
Cohort
Time Perspective
Prospective

Eligibility Criteria

Ages
1 Day to 18 Years (Child, Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •Children undergoing external ventricular drainage

Exclusion Criteria

  • •Children who were intubated preoperatively.

Outcomes

Primary Outcomes

Anesthesia method

Time Frame: From enrollment to the end of surgery

The anesthesia method used for the surgery (general anesthesia or sedation)

Secondary Outcomes

  • Analgesic consumption(Postoperative first 24 hours.)

Investigators

Sponsor
Hande Gurbuz
Sponsor Class
Other Gov
Responsible Party
Sponsor Investigator
Principal Investigator

Hande Gurbuz

Assoc. Prof., MD, PhD

Bursa City Hospital

Study Sites (1)

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