Evaluation of Vidiac Scores of Obese and Non-obese Patients Intubated by Videolaryngoscopy

• Sponsor: Ankara City Hospital Bilkent (Other)
• Overall Status: Not yet recruiting
• CT.gov ID: NCT05697731
• 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 non-obese and obese patients and to reveal the differences, if any.

Condition or Disease	Intervention/Treatment	Phase
Vidiac Score; Videolaryngoscopy; Obesity	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 Non-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.
non-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 70 Years
• Sexes Eligible for Study: All
• Accepts Healthy Volunteers: Yes

Inclusion Criteria:

• All 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

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, Ankara City Hospital Bilkent
• ClinicalTrials.gov Identifier: NCT05697731
• Other Study ID Numbers: E2-22-2939
• 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

Study Results

No Results Posted as of Jan 26, 2023