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Goal-directed Low Oxygen During Anesthesia

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

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05263154
Enrollment
200
Registered
2022-03-02
Start date
2022-03-28
Completion date
2025-03-31
Last updated
2023-08-16

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Postoperative Complications

Keywords

postoperative hypoxia, abdominal surgery, randomized controlled trial

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.

Interventions

OTHERGoal directed low oxygen

Oxygen is titrated until oxygen saturation is 100% in one-minute steps 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.

OTHERHigh oxygen

FiO2 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%

Sponsors

Umeå University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Outcomes Assessor)

Intervention model description

Randomized controlled trial

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
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

Design outcomes

Primary

MeasureTime frameDescription
Mean change in arterial oxygen partial pressure after surgery vs. before surgery3 daysOxygen partial pressure

Secondary

MeasureTime frameDescription
Mean change in diffusion capacity for carbon-monoxide after surgery vs. before surgery3 daysDiffusion capacity
Mean change in vital capacity after surgery vs. before surgery3 daysVital capacity
Mean change in forced expiratory volume in one second after surgery vs. before surgery3 daysForced expiratory volume in one second
Mean change in arterial carbon-dioxide partial pressure after surgery vs. before surgery3 daysCarbon-dioxide partial pressure
Mean change in arterial oxygen partial pressure after surgery vs. before surgery3 monthsOxygen partial pressure

Countries

Sweden

Contacts

Primary ContactKarl A Franklin, MD, Prof
karl.franklin@umu.se+46 907851256

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026