Airway Management During TCI vs RSI Anesthesia Induction

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

70 participants

Study Classification

OBSERVATIONAL

Study Start Date

2018-10-29

Study Completion Date

2019-05-31

Brief Summary

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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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Detailed Description

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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.

Conditions

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Adverse Effect Anesthesia Airway Complication of Anesthesia

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Interventions

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Induction of anesthesia

Standardized TCI and RSI anesthesia induction

Intervention Type PROCEDURE

Other Intervention Names

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Anesthesia induction

Eligibility Criteria

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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

Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No