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Clinical Trials/NCT05263154
NCT05263154RecruitingNot Applicable

Goal-directed Low vs. High Oxygen Therapy During Anesthesia for Abdominal Surgery

Umeå University1 site in 1 country200 target enrollmentStarted: March 28, 2022Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Recruiting
Enrollment
200
Locations
1
Primary Endpoint
Mean change in arterial oxygen partial pressure after surgery vs. before surgery

Study Overview

Brief Summary

The study aims at investigate whether low oxygen therapy during anesthesia improves oxygen partial pressure and lung function in the postoperative period after abdominal surgery. 200 patients scheduled for abdominal surgery will be randomized (1:1) to goal directed low oxygen concentration during and after anesthesia vs. fixed high oxygen concentration. Arterial oxygen partial pressure is the primary outcome and lung function a secondary explanatory outcome.

Detailed Description

Postoperative hypoxia is a most common complication after major abdominal surgery. This study aims at investigate whether goal-directed low oxygen therapy during anesthesia improves oxygen partial pressure and lung function in the postoperative period after abdominal surgery.

200 adult patients scheduled for major abdominal cancer surgery lasting for more than 2 hours will be included after signed informed consent. Patients will then be randomized to either goal directed low oxygen or high oxygen during anesthesia and in the postoperative period.

Patients who are randomized to goal directed low oxygen will be given oxygen before the induction of anesthesia, with increasing fraction of inspired oxygen (FiO2) from 0.25 to 0.30 to 0.35 and so on. After intubation, the FiO2 is set to 0.25 to achieve a target saturation of 94-96%. Supplementary oxygen after surgery will be given with the same targets and with as little oxygen as necessary, Patients who are randomized to high oxygen will be given FiO2 of 1.0 before induction until end-tidal oxygen concentrations of 0.80 occur. The FiO2 will be reduced to 0.35 during anesthesia, followed by an increase in FiO2 to 0.80 during 5 minutes before extubating the patient, followed by FiO2 0.40 for at least thirty minutes after anesthesia. Oxgen will then be given at 3 liters a minute with a oxygen saturation goal of 98%.

Arterial blood gases, lung function measurements including diffusion capacity will be taken on the day before surgery. Blood gases will be taken during the first and second day after surgery and lung function tests during the second day after surgery. Blood gases and lung function will also be obtained at three months after surgery.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
Double (Participant, Outcomes Assessor)

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •Being scheduled for a major abdominal cancer surgery lasting for more than 2 hours.
  • •Having a condition within American Society of Anesthesia Class 1-3.

Exclusion Criteria

  • •Being at risk for a difficult intubation during anesthesia in the form of Mallampati score 3-4, or having a previous documentation of difficult intubation.
  • •Decline participation

Arms & Interventions

Goal directed low oxygen

Experimental

Oxygen given at low concentrations following goals of oxygen saturation during and after anesthesia

Intervention: Goal directed low oxygen (Other)

High oxygen

Active Comparator

Oxygen given as traditionally including high concentrations

Intervention: High oxygen (Other)

Outcomes

Primary Outcomes

Mean change in arterial oxygen partial pressure after surgery vs. before surgery

Time Frame: 3 days

Oxygen partial pressure

Secondary Outcomes

  • Mean change in vital capacity after surgery vs. before surgery(3 months)
  • Mean change in forced expiratory volume in one second after surgery vs. before surgery(3 months)
  • Mean change in arterial carbon-dioxide partial pressure after surgery vs. before surgery(3 months)
  • Mean change in diffusion capacity for carbon-monoxide after surgery vs. before surgery(3 months)
  • Mean change in arterial oxygen partial pressure after surgery vs. before surgery(3 months)
  • Mean change in diffusion capacity for carbon-monoxide after surgery vs. before surgery(3 days)
  • Mean change in vital capacity after surgery vs. before surgery(3 days)
  • Mean change in forced expiratory volume in one second after surgery vs. before surgery(3 days)
  • Mean change in arterial carbon-dioxide partial pressure after surgery vs. before surgery(3 days)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Karl A Franklin

Profesor, Consultant surgeon

Umeå University

Study Sites (1)

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