Evaluation of Complications in Airway Management
AMC
Evaluation of Complications During Airway Management: An Observational Prospective Cohort Study
1 other identifier
observational
1,000
1 country
1
Brief 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)
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Jan 2018
Shorter than P25 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
January 1, 2018
CompletedFirst Submitted
Initial submission to the registry
May 27, 2018
CompletedFirst Posted
Study publicly available on registry
June 8, 2018
CompletedPrimary Completion
Last participant's last visit for primary outcome
July 1, 2018
CompletedStudy Completion
Last participant's last visit for all outcomes
July 1, 2018
CompletedJuly 11, 2018
July 1, 2018
6 months
May 27, 2018
July 10, 2018
Conditions
Keywords
Outcome Measures
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
6 months
Secondary Outcomes (3)
variety of complications and reasons of the complications
6 months
preventable reasons of the complications
6 months
the time at which complications occurs more, during airway management
6 months
Study Arms (1)
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.
Interventions
patients will be intubated or will be placed an airway device
Eligibility Criteria
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
You may qualify if:
- Patients undergoing general anesthesia
- Patients to whom airway devices will be inserted
You may not qualify if:
- Patients who undergo surgery under regional anesthesia
- Patients who undergo surgery under sedation
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Derince Research and Training Hospital
Kocaeli, 41900, Turkey (Türkiye)
MeSH Terms
Interventions
Intervention Hierarchy (Ancestors)
Study Officials
- STUDY DIRECTOR
tolga k saracoglu, assoc. prof.
Sağlık Bilimleri Üniversitesi Kocaeli Derince SUAM
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Principle Investigator
Study Record Dates
First Submitted
May 27, 2018
First Posted
June 8, 2018
Study Start
January 1, 2018
Primary Completion
July 1, 2018
Study Completion
July 1, 2018
Last Updated
July 11, 2018
Record last verified: 2018-07