Impact of Intraoperative Oxygenation Practices on Patient Outcomes
Recruiting
N/AInterventional Study
Surgeries Undergoing General Anesthesia
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
Ready to participate?
Review the details below, then apply to join this clinical trial.
At a Glance
Age
18 and older
Sex
Any
Study type
Interventional
Purpose
Treatment
Participants needed
54,000 (estimated)
Sponsor
Frederic T Billings IV · Other
Who this trial is looking for
This trial is looking for adult patients who are having surgery that requires general anesthesia. Participants will be part of a study that tests different oxygen levels used during surgery to see how they affect recovery outcomes.
Are You a Good Fit for This Trial?
You may be able to join if
I am at a hospital where this trial is taking place.
I have a planned surgery that involves putting me under general anesthesia.
You may not be able to join if
I am under 18 years old.
I am pregnant.
I am a prisoner.
I am classified as an organ donor.
My surgery involves open heart surgery.
My procedure requires prolonged apnea or special airway procedures.
My surgery involves using ECMO.
I have a history of bleomycin treatment.
Summarized in plain language from this trial's official eligibility criteria.
The full criteria are further down this page — only the research team can
confirm whether you qualify.
Think this trial could be right for you?
Answer three quick questions written from this study's own rules to see if you may qualify. No account needed to find out.
This multicenter, cluster-randomized, cluster-crossover clinical trial evaluates the impact of three intraoperative FiO2 (Fraction of Inspired Oxygen) oxygenation strategies-lower (FiO₂ 0.21-0.40), intermediate (FiO₂ 0.40-0.80), and higher (FiO₂ 0.80-1.00)-on postoperative organ injury and mortality in adult surgical patients. The trial aims to determine the optimal oxygenation strategy to improve…
This multicenter, cluster-randomized, cluster-crossover clinical trial evaluates the impact of three intraoperative FiO2 (Fraction of Inspired Oxygen) oxygenation strategies-lower (FiO₂ 0.21-0.40), intermediate (FiO₂ 0.40-0.80), and higher (FiO₂ 0.80-1.00)-on postoperative organ injury and mortality in adult surgical patients. The trial aims to determine the optimal oxygenation strategy to improve perioperative outcomes.
Trial Locations
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Status
Eligibility Criteria
Inclusion Criteria:
* Patient located in a participating operating room
* Planned surgery includes tracheal intubation
Exclusion Criteria:
* Patient is known to be less than 18 years old
* Patient is known to be pregnant
* Patient is known to be a prisoner.
* Patient is American Society of Anesth…
Inclusion Criteria:
* Patient located in a participating operating room
* Planned surgery includes tracheal intubation
Exclusion Criteria:
* Patient is known to be less than 18 years old
* Patient is known to be pregnant
* Patient is known to be a prisoner.
* Patient is American Society of Anesthesiologists (ASA) classification-6 (i.e., organ donor)
* Patient's planned surgical case includes open heart surgery, defined as surgery on the heart or ascending aorta requiring sternotomy or thoracotomy.
* Patient's planned procedure requires prolonged apnea, bronchoscopy, airway surgery, or one-lung ventilation.
* Patient's planned surgical case includes use of extracorporeal membrane oxygenation (ECMO).
* Patient is known to have a history of bleomycin treatment.
* Patient was enrolled in the trial in the prior 30 days.
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