Evaluation of Vidiac Scores of Obese and Non-obese Patients Intubated by Videolaryngoscopy
1 other identifier
observational
82
1 country
1
Brief Summary
The aim of the study was to observe the vidiac score values of only patients with obesity as a risk factor for difficult intubation. Secondly, it was aimed to evaluate the number of intubation attempts and intubation time, vidiac scores between non-obese and obese patients and to reveal the differences, if any.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for all trials
Started Feb 2023
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
First Submitted
Initial submission to the registry
January 15, 2023
CompletedFirst Posted
Study publicly available on registry
January 26, 2023
CompletedStudy Start
First participant enrolled
February 1, 2023
CompletedPrimary Completion
Last participant's last visit for primary outcome
April 1, 2023
CompletedStudy Completion
Last participant's last visit for all outcomes
September 1, 2023
CompletedJanuary 26, 2023
January 1, 2023
2 months
January 15, 2023
January 15, 2023
Conditions
Outcome Measures
Primary Outcomes (1)
vidiac score
Vidiac score is a scoring system created according to the visibility of laryngeal structures under videoingoscopy in patients with expected difficult intubation.
during entubation
Study Arms (2)
obese
Vidiac score Mallampati score upper lip bite test Thyromental distance Mandible ramus length Mouth opening distance
non-obese
Vidiac score Mallampati score upper lip bite test Thyromental distance Mandible ramus length Mouth opening distance
Interventions
Vidiac score is a scoring system created according to the visibility of laryngeal structures under videolarnyngoscopy in patients with expected difficult intubation.
Eligibility Criteria
patients to be operated under general anesthesia and endotracheal intubation
You may qualify if:
- All patients to be operated under general anesthesia and endotracheal intubation
You may not qualify if:
- under 18 years old
- The patient's refusal
- Difficult airway story before
- Congenital or previous airway anatomical disorder
- Patients who have undergone airway surgery
- Patients with a mass in the head and neck region
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Ankara City Hospital
Ankara, Turkey (Türkiye)
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Aysun Postacı, Assoc. Prof
Ankara City Hospital Bilkent
Central Study Contacts
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- PROSPECTIVE
- Target Duration
- 7 Months
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Ankara City Hospital
Study Record Dates
First Submitted
January 15, 2023
First Posted
January 26, 2023
Study Start
February 1, 2023
Primary Completion
April 1, 2023
Study Completion
September 1, 2023
Last Updated
January 26, 2023
Record last verified: 2023-01