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Completed

NCT Number: NCT03723109

Airway Management During TCI vs RSI Anesthesia Induction

The aims of this observational study is to evaluate and compare feasibility of airway management during standardized TCI and RSI anesthesia induction.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Sunderby teaching hospital

Luleå, 97180, Sweden

About this study

The aims of this study are to evaluate and compare feasibility of airway management and risk for desaturation during standardized target controlled infusion (TCI) and rapid sequence induction (RSI) of anesthesia. A conventional way to induce anesthesia, i.e. manual injection of anesthetics, may be more accurate and predictable compared to dosing regimes based on complex mathematical algorithms used in TCI-systems. In addition, today many different models are presented and there is no consensus which kind of TCI-algorithm should be used universally. Moreover, dosing algorithms are most complex and challenging in underweight and morbid obesity. There are many publications on this field, but no data of feasibility of airway management can be found. Indeed, RSI induction is traditionally blamed to be risky and not recommended as a first choice.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • signed informed consent
  • BMI < 35 kg/m2
  • preoperative assessment accepted by consultant anesthesiologist
  • scheduled for breast cancer surgery, endocrinological surgery (thyroid, parathyroid) or minor general abdominal surgery.

Exclusion criteria

  • not signed consent
  • instable angina pectoris
  • severe bronchial asthma
  • severe chronic obstructive pulmonary disease
  • dementia
  • severe heart valve disease
  • severe renal failure
  • body mass index > 35 kg/m2

Treatment and study plan

Induction of anesthesia

Procedure

Standardized TCI and RSI anesthesia induction

Other names: Anesthesia induction

Primary outcomes

  1. Safety time for apnea

    Time frame: 10min

    measurement of length of period for apnea during TCI and RSI induction by a timer

Secondary outcomes

  1. Duration of spontaneous breathing

    Time frame: 10min

    measurement of duration of spontaneous breathing during TCI and RSI induction by a timer

Sponsors and collaborators

Lead sponsor

Umeå University

Other

Registry information

Official study title

Airway Management and Safety Aspects During Target Controlled Infusion (TCI) Compared to Rapid Sequence Induction (RSI) of Anesthesia in Non-cardiac Surgery

Important dates

Study start
2018
Primary completion
2019
Study completion
2019
First posted
Oct 29, 2018
Registry last updated
Sep 26, 2019

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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