Skip to content

Retrospective Study in Patients Who Have Had a Difficult Intubation.

Retrospective Study of the Risk of Aspiration and Postoperative Pulmonary Problems in Patients Who Have Had a Difficult Intubation.

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02576756
Enrollment
1000
Registered
2015-10-15
Start date
2015-10-31
Completion date
2016-06-30
Last updated
2025-11-18

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

Conditions

Aspiration, Pneumonia

Keywords

Risk on aspiration, Postoperative, Difficult Intubation

Brief summary

The investigator wants to investigate if there is an increased risk of postoperative pulmonary problems in patients who have had an intubation where there was need for more than a laryngoscope.

Detailed description

A difficult intubation is defined as an intubation in which more than a laryngoscope was needed. Afterwards patient data retrieved from the Clinical Work Station: age, type of operation and time, date, type of anaesthesia, de tools needed for intubation, time needed for intubation and anaesthesia. In the Clinical Work Station of the Hospital the investigator will search for the following data in these selected patients: preoperative comorbidities, home medication, type of postoperative pulmonary problems and the treatment that was given, time of hospital stay and which department the patient stayed. Patients with a difficult intubation will be linked to a patient with a corresponding medical history and type of operation but without a difficult intubation. The investigator will look for the same parameters of these patients in the Clinical Work Station. By means of an odds-ratio the relative risk of a pulmonary complication after a difficult intubation in connection with an easy intubation with different variables can be calculated.

Interventions

None listed

Sponsors

Universitair Ziekenhuis Brussel
Lead SponsorOTHER

Study design

Observational model
CASE_CONTROL
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

* Every patient who had an intubation where another device than a laryngoscope was necessary

Exclusion criteria

* N/A

Design outcomes

Primary

MeasureTime frameDescription
Relative risk for postoperative pulmonary incidents6 monthsnumber of participants with Relative risk

Outcome results

None listed

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