Evaluation of Vidiac Scores of Obese and Morbid Obese Patients Intubated by Videolaryngoscopy

• Sponsor: Ankara City Hospital Bilkent (Other)
• Overall Status: Not yet recruiting
• CT.gov ID: NCT05697744
• Collaborator: (none)
• Enrollment: 82
• Location: 1
• Anticipated Duration (Months): 7
• Patients Per Site Per Month: 11.8

Study Details

Study Description

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 obese and morbid obese patients and to reveal the differences, if any.

Condition or Disease	Intervention/Treatment	Phase
Vidiac Score; Videolaryngoscopy; Obesity, Morbid	Diagnostic Test: Vidiac Score

Study Design

• Study Type: Observational [Patient Registry]
• Anticipated Enrollment: 82 participants
• Observational Model: Cohort
• Time Perspective: Prospective
• Official Title: Evaluation of Vidiac Scores of Obese and Morbid Obese Patients Intubated by Videolaryngoscopy
• Anticipated Study Start Date: Feb 1, 2023
• Anticipated Primary Completion Date: Apr 1, 2023
• Anticipated Study Completion Date: Sep 1, 2023

Arms and Interventions

Arm	Intervention/Treatment
obese Vidiac score Mallampati score upper lip bite test Thyromental distance Mandible ramus length Mouth opening distance	Diagnostic Test: Vidiac Score; Vidiac score is a scoring system created according to the visibility of laryngeal structures under videolarnyngoscopy in patients with expected difficult intubation.
Morbid obese Vidiac score Mallampati score upper lip bite test Thyromental distance Mandible ramus length Mouth opening distance	Diagnostic Test: Vidiac Score; Vidiac score is a scoring system created according to the visibility of laryngeal structures under videolarnyngoscopy in patients with expected difficult intubation.

Outcome Measures

Primary Outcome Measures

1. vidiac score [during entubation]

   Vidiac score is a scoring system created according to the visibility of laryngeal structures under videoingoscopy in patients with expected difficult intubation.

Eligibility Criteria

Criteria

• Ages Eligible for Study: 18 Years to 80 Years
• Sexes Eligible for Study: All
• Accepts Healthy Volunteers: Yes

Inclusion Criteria:

• All obese and morbidly obese patients to be operated under general anesthesia and endotracheal intubation

Exclusion Criteria:

1. under 18 years old

2. The patient's refusal

3. Difficult airway story before

4. Congenital or previous airway anatomical disorder

5. Patients who have undergone airway surgery

6. Patients with a mass in the head and neck region

7. Body mass ındex < 30 kg/m2

Contacts and Locations

Locations

	Site	City	State	Country	Postal Code
1	Ankara City Hospital	Ankara		Turkey

Sponsors and Collaborators

• Ankara City Hospital Bilkent

Investigators

• Principal Investigator: Aysun Postacı, Assoc. Prof, Ankara City Hospital Bilkent

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.

• Responsible Party: aysun postaci, Ankara City Hospital Bilkent, Ankara City Hospital Bilkent
• ClinicalTrials.gov Identifier: NCT05697744
• Other Study ID Numbers: E2-23-3157
• First Posted: Jan 26, 2023
• Last Update Posted: Jan 26, 2023
• Last Verified: Jan 1, 2023

• Individual Participant Data (IPD) Sharing Statement: Undecided
• Plan to Share IPD: Undecided
• Studies a U.S. FDA-regulated Drug Product: No
• Studies a U.S. FDA-regulated Device Product: No
• Additional relevant MeSH terms: Obesity, Morbid

Study Results

No Results Posted as of Jan 26, 2023