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CompletedNCT03550326AMCUpdated Jul 11, 2018

Evaluation of Complications in Airway Management

An observational study in Airway Complication of Anesthesia and Difficult Intubation, sponsored by Derince Training and Research Hospital. Completed at 1 site in Turkey. Per ClinicalTrials.gov, last updated 2018-07-11.

Sponsored by Derince Training and Research Hospital · Observational

Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
1,000
Sex
All
01

Study summary

In the current study researchers aim to evaluate the rate of the complication due to airway management (during intubation or placement of supraglottic airway devices)

Read the detailed description

Airway management is one of the most important subject of anesthesia practice. Airway devices ,helping anesthesiologists to maintain airway safety have many complications. 4 th national audit project (NAP 4) study was designed to evaluate the incidence of the major complication of airway management. Accordingly in current study authors aim to determine the complications and incidence of the complications during airway management.

02

Conditions studied

  • Airway Complication of Anesthesia
  • Difficult Intubation

Keywords

  • anesthesia
  • difficult airway
  • supraglottic airway device
  • difficult intubation
  • airway complications
03

In context

Lead sponsor

Derince Training and Research Hospital is the lead sponsor of 39 studies on the registry; none are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
Child (0–17), Adult (18–64), Older adult (65+)
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

patients who undergo surgery under general anesthesia and who intubate/place supraglottic airway device will be recruit for study over a period of six months

Inclusion criteria

  • Patients undergoing general anesthesia
  • Patients to whom airway devices will be inserted

Exclusion criteria

Exclusion Criteria:

  • Patients who undergo surgery under regional anesthesia
  • Patients who undergo surgery under sedation
05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
1,000 participants (actual)
Patient registry
No

Groups and cohorts

  • general anesthesia

    Patients who undergo general anesthesia and are intubated or inserted airway device will be enrolled. researchers will follow the induction and intubation period and record all the complications due to airway management.

    Procedure: airway management

Interventions

  • Procedureairway management

    patients will be intubated or will be placed an airway device

06

What researchers measure

Primary outcomes

  1. The incidence of the complications due to airway management

    researchers will observe the whole patients who undergo general anesthesia and record the data

    Time frame: 6 months

Secondary outcomes

  1. variety of complications and reasons of the complications

    researchers will observe the whole patients who undergo general anesthesia and record the data

    Time frame: 6 months

  2. preventable reasons of the complications

    researchers will observe the whole patients who undergo general anesthesia and record the data

    Time frame: 6 months

  3. the time at which complications occurs more, during airway management

    researchers will observe the whole patients who undergo general anesthesia and record the data

    Time frame: 6 months

07

Study locations

1 site
  • Derince Research and Training Hospital
    Kocaeli, 41900, Turkey
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jul 11, 2018, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT03550326
Lead sponsor
Derince Training and Research Hospital
Responsible party
Ayse Zeynep Turan (Principle Investigator, Derince Training and Research Hospital) — Principal investigator
First posted
Jun 8, 2018
Start date
Jan 1, 2018
Primary completion
Jul 1, 2018
Completion
Jul 1, 2018
Last update
Jul 11, 2018

Study contacts

tolga k saracoglu, assoc. prof.
study director · Sağlık Bilimleri Üniversitesi Kocaeli Derince SUAM

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Jul 2018. You cannot join it, but the record below documents what was studied.

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