Tighter oxygen control tested for COPD patients on breathing machines
NCT ID NCT07842510
First seen Sep 25, 2026 · Last updated Sep 25, 2026
Summary
Researchers are testing whether keeping blood oxygen levels between 88% and 92% helps ICU patients with acute exacerbations of COPD. The trial compares this controlled oxygen strategy with standard care, which aims for oxygen levels above 94%. The main goal is to see if controlled oxygen reduces the total time patients need mechanical ventilation, with secondary checks on 28-day mortality, ICU stay length, and complications from too much oxygen. The study enrolls 240 adults aged 40 and older admitted to the ICU for a COPD flare-up.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- controlled oxygen therapy, where oxygen delivery is adjusted to keep blood oxygen saturation between 88% and 92%
- What this could lead to
- If controlled oxygen therapy helps, it could shorten the time patients spend on breathing machines and reduce deaths in the ICU. It could also give critical care teams a clearer target for oxygen levels in COPD flare-ups.
- What could go wrong
- This is a single trial in one hospital system, so results may not apply everywhere. Oxygen targets are hard to keep steady in very sick patients, and the study may not show a clear difference between the two approaches.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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About 240 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Jan 2026
- Expected to finish
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Dec 2028
An estimate. End dates often move.
- Lead sponsor
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A government agency
The lead sponsor is a government body.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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40 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Age ≥ 40 years * Established diagnosis of chronic obstructive pulmonary disease (COPD) according to the Global Initiative for Chronic Obstructive Lung Disease (GOLD) criteria * Admission to the intensive care unit for an acute exacerbation of COPD, with or without respiratory acidosis * Written informed consent provided by the participant or their legally authorized representative Exclusion Criteria: * Endotracheal intubation performed before enrollment * Severe decompensated heart failure with a left ventricular ejection fraction \< 30% * Active terminal malignancy * Refusal to participate in the study
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
2 sites. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Dhouha Ben Braiek
NOT_YET_RECRUITINGKairouan, Tunisia
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Taher Sfar Mahdia Hospital
RECRUITINGMahdia, Mahdia Governorate, 5100, Tunisia
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