Informations générales (source: ClinicalTrials.gov)

NCT06421012 En recrutement IDF
Preoxygenation for Tracheal Aspirations in Intensive Care, a Randomized Controlled Trial
Interventional
N/A
Assistance Publique - Hôpitaux de Paris (Voir sur ClinicalTrials)
janvier 2025
décembre 2027
13 septembre 2025
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 These longstanding recommendations were reiterated in 2022, based on outdated studies involving systematic suctioning that required disconnecting the patient from the ventilator.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.
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Etablissements

Les établissements d'Île-de-France ayant mis à jour leurs données Origine et niveau de fiabilité des données
GHEM SIMONE VEIL SITE EAUBONNE CHRETIEN Manon En recrutement IDF 18/09/2025 17:35:10  Contacter
GHI LE RAINCY MONTFERMEIL CHRETIEN Manon En recrutement IDF 18/09/2025 17:35:10  Contacter
AP-HP Assistance publique - Hôpitaux de Paris En recrutement IDF 18/09/2025 17:35:11  Contacter
AP-HP - Hôpital Beaujon
AP-HP - Hôpital Bicêtre
AP-HP - Hôpital Henri Mondor-Albert Chenevier
AP-HP - Hôpital La Pitié-Salpêtrière
AP-HP - Hôpital Lariboisiere-Fernand Widal
AP-HP - Hôpital Saint Antoine
AP-HP - Hôpital Saint Louis
Les établissements hors Île-de-France dont les données sont issues de ClinicalTrials.gov Origine et niveau de fiabilité des données
18/09/2025 17:35:10 Contact (sur clinicalTrials)
18/09/2025 17:35:10 Contact (sur clinicalTrials)
18/09/2025 17:35:10 Contact (sur clinicalTrials)
18/09/2025 17:35:10 Contact (sur clinicalTrials)
18/09/2025 17:35:10 Contact (sur clinicalTrials)
18/09/2025 17:35:10 Contact (sur clinicalTrials)
18/09/2025 17:35:10 Contact (sur clinicalTrials)
18/09/2025 17:35:10 Contact (sur clinicalTrials)
18/09/2025 17:35:10 Contact (sur clinicalTrials)
18/09/2025 17:35:10 Contact (sur clinicalTrials)
18/09/2025 17:35:10 Contact (sur clinicalTrials)
18/09/2025 17:35:10 Contact (sur clinicalTrials)
18/09/2025 17:35:11 Contact (sur clinicalTrials)
Les établissements sans correspondance certaine dans le répertoire FINESS dont les données sont issues de ClinicalTrials.gov Origine et niveau de fiabilité des données
Hôpital Pitié Salpêtrière - 75013 - Paris - France Claire FAZILLEAU En recrutement Contact (sur clinicalTrials)

Critères

Tous
Inclusion Criteria:

- 18 years of age or older

- Hospitalized in ICU, under invasive mechanical ventilation for less than 24 hours

- Information and signature of consent by patient or relative/trusted person, or
emergency inclusion procedure



- Patient on ECMO

- Not affiliated to a social security system

- Pregnant

- Under legal protection (curatorship, guardianship or safeguard of justice)

- Patient under AME

- Patient included in another interventional study that may have an impact on the
evaluation criteria of the present study