Actively Recruiting

Phase Not Applicable
Age: 3Years - 11Years
All Genders
Healthy Volunteers
NCT06303518

End Tidal Carbon Dioxide Concentration and Depth of Anesthesia in Children

Led by University of British Columbia · Updated on 2025-03-25

100

Participants Needed

1

Research Sites

127 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Carbon Dioxide (CO2) is a by-product of metabolism and is removed from the body when we breathe out. High levels of CO2 can affect the nervous system and cause us to be sleepy or sedated. Research suggests that high levels of CO2 may benefit patients who are asleep under anesthesia, such as by reducing infection rates, nausea, or recovery from anesthesia . CO2 may also reduce pain signals or the medication required to keep patients asleep during anesthesia; this has not been researched in children. During general anesthesia, anesthesiologists keep patients asleep with anesthetic gases or by giving medications into a vein. These drugs can depress breathing; therefore, an anesthesiologist will control breathing (ventilation) with an artificial airway such as an endotracheal tube. Changes in ventilation can alter the amount of CO2 removed from the body. The anesthesiologist may also monitor a patient's level of consciousness using a 'Depth of Anesthesia Monitor' such as the Bispectral Index (BIS), which analyzes a patient's brain activity and generates a number to tell the anesthesiologist how asleep they are. The investigator's study will test if different levels of CO2 during intravenous anesthesia are linked with different levels of sedation or sleepiness in children, as measured by BIS. If so, this could reduce the amount of anesthetic medication the child receives. Other benefits may be decreased medication costs, fewer side effects, and a positive environmental impact by using less disposable anesthesia equipment.

CONDITIONS

Official Title

End Tidal Carbon Dioxide Concentration and Depth of Anesthesia in Children

Who Can Participate

Age: 3Years - 11Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Children aged 3 to 11 years undergoing non- or minimally-stimulating elective procedures without painful manipulation
  • American Society of Anesthesiologists (ASA) physical status I or II
  • Use of total intravenous anesthesia (TIVA) for induction and maintenance
  • Controlled ventilation using an endotracheal tube
  • Anticipated surgery time of 90 minutes or longer to allow testing at all three CO2 levels
Not Eligible

You will not qualify if you...

  • Need for inhalational induction of anesthesia
  • Use of sedative premedication
  • Use of ketamine during surgery
  • Inability to place BIS electrodes due to surgery site or contraindications
  • Allergy to propofol, remifentanil, or lidocaine
  • Depression of consciousness for any reason
  • Body mass index below 5th or above 95th percentile for age
  • History of obstructive or central sleep apnea
  • Known or suspected raised intracranial pressure
  • Recent or previous traumatic brain injury

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

BC Children's Hospital

Vancouver, British Columbia, Canada, V6H 3N1

Actively Recruiting

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Research Team

V

Victoria Buswell

CONTACT

S

Steffanie Fisher

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

CROSSOVER

Primary Purpose

OTHER

Number of Arms

6

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