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Iterative Endotracheal Tube Cuff Pressure Monitoring

Iterative Endotracheal Tube Cuff Pressure Monitoring

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05889611
Acronym
SIPBIE
Enrollment
100
Registered
2023-06-05
Start date
2023-03-22
Completion date
2024-03-22
Last updated
2023-06-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Spine Disease

Keywords

Spine Disease, Spine surgery, Intubation Cuff Pressure, Endotracheal Intubation, Upper airways

Brief summary

Studies in the medical literature underline the importance of monitoring the pressure of the balloon and the relationship with the incidence cited on the pain and discomfort related to the gesture of the upper airways. There are no formal recommendations in the literature, the French Society of Anesthesia and Resuscitation (SFAR) recommends monitoring the pressure intraoperatively except after intubation. It would be interesting to see and thus make an inventory of the practices, to reiterate the importance of monitoring throughout the gesture and at the change of position to avoid either micro-inhalation linked to under pressure of the balloon or overpressure which causes a potential risk of tracheal injury.

Interventions

None listed

Sponsors

University Hospital, Strasbourg, France
Lead SponsorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum

Inclusion criteria

* Elderly patient ≥ 18 years old * Patient who has a scheduled spine intervention in the prone position from January 1, 2023 to April 30, 2023 * Intubated patient with endotracheal tube under mechanical ventilation * Sedation and curarization * ASA 1, 2 and 3 * Duration of surgery \> 1 hour * Subject not objecting to the reuse of their data for the purposes of this research.

Exclusion criteria

* Subject who expressed their opposition to participating in the study * ASA 4, difficult intubation and emergency * Lung pathologies (asthma, COPD, tracheomalacia) * Severe heart failure * Septic, cardiogenic or volume shock * Morbid obesity (BMI \>40)

Design outcomes

Primary

MeasureTime frameDescription
Balloon pressureThroughout the surgical procedureMonitoring of balloon pressure following prone position during spine surgery

Countries

France

Contacts

Primary ContactNicolas PARTOUCHE, MD
nicolas.partouche@chru-strasbourg.fr33 3 68 76 51 09

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026