NCT02576756

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.

Trial Health

100
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
1,000

participants targeted

Target at P75+ for all trials

Timeline
Completed

Started Oct 2015

Shorter than P25 for all trials

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

October 1, 2015

Completed
12 days until next milestone

First Submitted

Initial submission to the registry

October 13, 2015

Completed
2 days until next milestone

First Posted

Study publicly available on registry

October 15, 2015

Completed
8 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

June 1, 2016

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

June 1, 2016

Completed
Last Updated

November 18, 2025

Status Verified

August 1, 2016

Enrollment Period

8 months

First QC Date

October 13, 2015

Last Update Submit

November 14, 2025

Conditions

AspirationPneumonia

Keywords

Risk on aspirationPostoperativeDifficult Intubation

Outcome Measures

Primary Outcomes (1)

  • Relative risk for postoperative pulmonary incidents

    number of participants with Relative risk

    6 months

Study Arms (2)

with difficult intubation

Control population

without difficult intubation

Control population

Eligibility Criteria

Sexall
Healthy VolunteersNo
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

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

You may qualify if:

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

You may not qualify if:

  • N/A

Contact the study team to confirm eligibility.

Sponsors & Collaborators

MeSH Terms

Conditions

Pneumonia

Condition Hierarchy (Ancestors)

Respiratory Tract InfectionsInfectionsLung DiseasesRespiratory Tract Diseases

Study Officials

  • Josia B Glissenaar, Med student

    Universitair Ziekenhuis Brussel

    PRINCIPAL INVESTIGATOR

  • Jan Poelaert, PhD MED

    Universitair Ziekenhuis Brussel

    STUDY CHAIR

Study Design

Study Type
observational
Observational Model
CASE CONTROL
Time Perspective
RETROSPECTIVE
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

October 13, 2015

First Posted

October 15, 2015

Study Start

October 1, 2015

Primary Completion

June 1, 2016

Study Completion

June 1, 2016

Last Updated

November 18, 2025

Record last verified: 2016-08

Data Sharing

IPD Sharing
Will not share