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Oxygenation by 100% Oxygen Via High Flow Nasal Cannula in Surgical Patients

K

Karolinska University Hospital

Status

Completed

Conditions

Ventilation
Anaesthesia, General
Anesthesia, Intravenous

Treatments

Procedure: Hyperventilation

Study type

Interventional

Funder types

Other

Identifiers

NCT02706431
Apnoic Oxygenation

Details and patient eligibility

About

Oxygenation with high-flow nasal cannula with 100% oxygen has only been evaluated in a limited number of studies. Although data are convincing it is of importance to evaluate this new concept in our department before implementing it into clinical practice.

The general purpose of this project is to evaluate a new ventilation strategy during ENT-surgery based on oxygenation with high-flow nasal cannula with 100% oxygen with focus on gas exchange.

Enrollment

31 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. Adult, >18 years old
  2. ENT-surgery where apnea is of benefit for the surgeon (eg. intraoral or laryngeal surgery) and the anesthesia time is <40 mins.
  3. Capable of understanding the study information and sign the written consent.

Exclusion criteria

  1. ASA>2
  2. NYHA >2
  3. BMI >30
  4. Pregnancy
  5. Manifest cardiac failure or coronary disease
  6. Neuromuscular disease

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

31 participants in 2 patient groups

Normoventilation
No Intervention group
Description:
The patients will be normoventilated before anesthesia
Hyperventilation
Experimental group
Description:
Prior to anesthesia, the patients will hyperventilate during 2 mins or until symptoms from the central nervous system (e.g. dizziness).
Treatment:
Procedure: Hyperventilation

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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