ClinicalTrials.Veeva

Menu

Pre-oxygenation Methods in Bariatric Patients

Imperial College London logo

Imperial College London

Status

Completed

Conditions

Bariatric Surgery Candidate
Obesity
Anesthesia

Treatments

Device: Standard anaesthetic face mask
Device: Optiflow and THRIVE technique

Study type

Interventional

Funder types

Other

Identifiers

NCT03428256
17SM3844

Details and patient eligibility

About

The purpose of the study is to compare effectiveness of different methods of achieving pre-oxygenation in bariatric patients. The investigators intend to compare facemask pre-oxygenation with a high-flow humidified nasal oxygen.

The primary outcome measure of interest is time to desaturation to 92% or 18 minutes of apnoea.

Full description

General anaesthesia involves giving patients anaesthetic and muscle relaxant medications to allow transition to sleep and airway relaxation to permit laryngoscopy, respectively. During laryngoscopy, a breathing tube is placed to 'secure' the airway. There is therefore a length of time from administration of these medications to when the breathing tube is placed, when the patient is not breathing and the airway is not secured. This time is known as apnoea time. In a patient who is not breathing, blood oxygen levels fall to dangerously-low levels, within 1-2 minutes. In order to prevent this, patients breathe 100% oxygen before induction of anaesthesia as part of a process known as pre-oxygenation. There are different ways of delivering pre-oxygenation, but the common aim is to increase the oxygen reservoir within the lungs to give the anaesthetist more time to place the breathing tube. With good pre-oxygenation, apnoea times of up to 7 minutes are possible.

Apnoea time is a potentially hazardous period during induction of anaesthesia and it is particularly so in patients with severe obesity. On the one hand, obesity makes the upper airway anatomy difficult, and on the other hand, lung collapse (atelectasis) caused by abdominal contents compressing the base of the lungs reduces the amount of oxygen available within the lungs. Apnoea time can be as short of 30 seconds. Identifying the most effective method of pre-oxygenating bariatric patients can therefore significantly improve the safety of delivering general anaesthesia to these patients.

Enrollment

80 patients

Sex

All

Ages

18 to 80 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Able to provide informed consent.
  • Undergoing general anaesthesia .
  • Between the ages of 18 and 80 years.
  • Body mass index (BMI) greater than 40 Kgm-2.

Exclusion criteria

  • Unable to give informed consent.
  • Significant cardiac history which is defined as current angina, myocardial infarction <12 months before the date of the procedure.
  • Significant peripheral vascular disease defined as claudication on minimal exertion or Ankle-Brachial index of <0.7, a stroke or a transient ischaemic attack <12 months before the procedure.
  • Presence of significant heart-valve disease or congestive heart failure.
  • Significant lower respiratory disease including brittle asthma; chronic obstructive pulmonary disease (GOLD stages 3 or 4).
  • Strong predictors of both difficult intubation and difficult facemask ventilation on anaesthetic airway assessment.
  • Patient with American Society of Anesthesiologists (ASA) grade of 4 for any reason.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

80 participants in 2 patient groups

Pre-oxygenation with a standard anaesthetic face mask
Active Comparator group
Description:
Pre-oxygenation delivered in the standard way; 3 minutes, Fraction of inspired oxygen (FiO2) 1.0, 8 vital capacity breaths in the last minute
Treatment:
Device: Standard anaesthetic face mask
Pre-oxygenation using Optiflow and THRIVE technique
Experimental group
Description:
Pre-oxygenation delivered via nasal high flow humidified oxygen (Optiflow) and THRIVE technique. Gradually increased to 70 litres/minute, mouth closed, 8 vital capacity breaths in the last minute
Treatment:
Device: Optiflow and THRIVE technique

Trial contacts and locations

1

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems