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Clinical Trials/NCT03723109
NCT03723109
Completed
Not Applicable

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

Umeå University1 site in 1 country70 target enrollmentOctober 29, 2018

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Adverse Effect
Sponsor
Umeå University
Enrollment
70
Locations
1
Primary Endpoint
Safety time for apnea
Status
Completed
Last Updated
6 years ago

Overview

Brief Summary

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

Detailed Description

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.

Registry
clinicaltrials.gov
Start Date
October 29, 2018
End Date
May 31, 2019
Last Updated
6 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Tomi Myrberg

Senior lecturer, MD PhD

Umeå University

Eligibility Criteria

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
  • severe heart valve disease
  • severe renal failure
  • body mass index \> 35 kg/m2

Outcomes

Primary Outcomes

Safety time for apnea

Time Frame: 10min

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

Secondary Outcomes

  • Duration of spontaneous breathing(10min)

Study Sites (1)

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