Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT06421012

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 These longstanding recommendations were reiterated in 2022, based on outdated studies involving systematic suctioning that required disconnecting the patient from the ventilator.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

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

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
Not Eligible

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

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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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