Status:

COMPLETED

Physiology Regarding Apnoeic Oxygenation During Nasal Cannula Therapy at Different Flow Rates

Lead Sponsor:

Insel Gruppe AG, University Hospital Bern

Conditions:

Apnoeic Oxygenation

Eligibility:

All Genders

18+ years

Phase:

NA

Brief Summary

This study compares under controlled conditions if different flow rates affect apnoea time after induction of anaesthesia and how CO2 clearance is influenced. Furthermore, this study enables to quanti...

Detailed Description

Eligible, consenting adults will be prepared for general anaesthesia in the usual way consisting of ECG, pulse-oximetry, NarcotrendTM, a venous cannula and an arterial line for continuous blood pressu...

Eligibility Criteria

Inclusion

  • \> 18 years
  • Written informed consent
  • Undergoing elective surgery
  • Requiring general anesthesia

Exclusion

  • Any Indication for fibre optic intubation
  • Expected impossible mask ventilation
  • Known coronary heart disease
  • Known heart failure, NYHA classification ≥ 2
  • Therapy including β-receptor antagonists
  • Arrhythmias in need of anti-arrhythmic therapy (e.g. implanted cardio defibrillator)
  • Peripheral occlusive arterial disease, Fontaine ≥ 2b
  • Known stenosis of the (common or internal) carotid or vertebral arteries
  • BMI \> 35kg/m2 and BMI \< 16kg/m2
  • Hyperkalaemia (K \> 5.5 mmol/l)
  • Known COPD Gold classification ≥ 2
  • Known pulmonary arterial hypertension, systolic \> 35mmHg
  • Known obstructive sleep apnoea syndrome in need of therapy
  • High risk of aspiration (requiring rapid sequence induction intubation)
  • Increased intracranial pressure
  • Intracranial surgery
  • Limited knowledge of German language
  • Absent power of judgement
  • Anaemia, Hb \< 100 g/l
  • Pregnancy (pregnancy test in all female patients)
  • Neuromuscular disorder
  • Known or suspected cervical spine instability
  • Nasal obstruction, impossibility of nasal ventilation (both sides patent)
  • Allergies or contra-indications to one or more of the used anaesthesia agents

Key Trial Info

Start Date :

March 25 2018

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

December 31 2019

Estimated Enrollment :

125 Patients enrolled

Trial Details

Trial ID

NCT03478774

Start Date

March 25 2018

End Date

December 31 2019

Last Update

February 3 2021

Active Locations (1)

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Page 1 of 1 (1 locations)

1

University Hospital Inselspital

Bern, Switzerland, 3008