Actively Recruiting
Preoxygenation for Tracheal Aspirations in Intensive Care
Led by Assistance Publique - Hôpitaux de Paris · Updated on 2025-05-11
2260
Participants Needed
1
Research Sites
152 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Clearing the airways is a complex phenomenon involving the production of secretions, the nature of mucus (viscosity, elasticity, stringiness, and adhesiveness), ciliary movement, and coughing. In intubated and ventilated patients, endotracheal suctioning occur when the patient is "unable to clear the airways of obstructions hindering the free passage of air." These suctioning can lead to transient desaturation exacerbated by a decrease in cardiac output due to increased mean arterial pressure, promoting cardiac arrhythmias. To minimize these effects, it is recommended to perform additional preoxygenation, by increasing the fraction of O2 in the air delivered to the patient by the ventilator 2-3 minutes before the procedure. These longstanding recommendations were reiterated in 2022, based on outdated studies involving systematic suctioning that required disconnecting the patient from the ventilator. Currently, suctioning are performed on-demand, based on the patient's congestion status, either through the endotracheal tube cap or a "closed system." Desaturations have become infrequent without establishing that additional preoxygenation can prevent them. Moreover, additional preoxygenation is not without risks. By inducing de-nitrogenation atelectasis with a loss of lung volume, it can exacerbate pre-existing lung injuries in the most severe patients. In less severe cases, preoxygenation leads to transient hyperoxia, with various deleterious effects impacting patient prognosis. Thus, a short-term risk, such as deep desaturations, must be balanced against a medium-term risk of hyperoxia and de-nitrogenation.
CONDITIONS
Official Title
Preoxygenation for Tracheal Aspirations in Intensive Care
Who Can Participate
Eligibility Criteria
You may qualify if you...
- 18 years of age or older
- Hospitalized in ICU, under invasive mechanical ventilation for less than 24 hours
- Provided informed consent by patient, relative, trusted person, or emergency inclusion procedure
You will not qualify if you...
- Receiving extracorporeal membrane oxygenation (ECMO)
- Not affiliated with a social security system
- Pregnant
- Under legal protection (curatorship, guardianship, or safeguard of justice)
- Under state medical aid (AME)
- Participating in another interventional study affecting this study's evaluation criteria
AI-Screening
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Trial Site Locations
Total: 1 location
1
Hôpital Pitié Salpêtrière
Paris, France, 75013
Actively Recruiting
Research Team
C
Claire FAZILLEAU
CONTACT
J
Jean Michel CONSTANTIN, Pr
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
SUPPORTIVE_CARE
Number of Arms
2
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