Expected Difficult Airway Management

NCT ID: NCT06279416

Last Updated: 2025-01-15

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

COMPLETED

Total Enrollment

49 participants

Study Classification

OBSERVATIONAL

Study Start Date

2023-12-30

Study Completion Date

2024-12-30

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

In this study, the investigators will evaluate the advanced airway methods applied in the anesthesiology and reanimation clinic of the hospital to patients who met the criteria for awake intubation specified in the ASA 2022 difficult airway management guideline or who could not be intubated after induction of anesthesia in another center. The advanced airway method applied to the difficult airway patient expected in the operating room, the duration, success and complications of the method will be observed and recorded.

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

Patients who meet the inclusion criteria will be informed about the difficult airway and their verbal and written consent will be obtained.

When participants are taken to the room, an observer will be in the operation room. There was no emergency to the patient's primary anesthesiologist, will not be involved. Record patients' demographic data, Mallampati scores, thyromental distance, and neck circumference.

The airway method preferred by the physician, procedure duration, number of attempts, success, and complications will be recorded.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Awake Intubation Advanced Airway Techniques

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

grup-1: awake nasal fiberoptic intubation

awake nasal fiberoptic intubation

fiberoptic intubation

Intervention Type PROCEDURE

awake nasal fiberoptic intubation

grup-2: awake intubation with laryngeal mask airway-mediated aintree catheter

awake intubation with laryngeal mask airway-mediated aintree catheter

laryngeal mask airway-mediated aintree catheter

Intervention Type PROCEDURE

awake intubation with laryngeal mask airway-mediated aintree catheter

grup-3: awake intubation with videolaryngoscopy

awake intubation with videolaryngoscopy

videolaryngoscopy

Intervention Type PROCEDURE

awake intubation with videolaryngoscopy

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

fiberoptic intubation

awake nasal fiberoptic intubation

Intervention Type PROCEDURE

laryngeal mask airway-mediated aintree catheter

awake intubation with laryngeal mask airway-mediated aintree catheter

Intervention Type PROCEDURE

videolaryngoscopy

awake intubation with videolaryngoscopy

Intervention Type PROCEDURE

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

* Over 18 years old
* Meets the expected difficult airway criteria
* Being awakened after induction of anesthesia in another center
* At least one of the awake intubation criteria in the DAS 2022 guideline
* Elective surgeries

Exclusion Criteria

* Emergency surgeries
* Patients intubated with anesthesia
* Noncoopere patients
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

Kocaeli City Hospital

OTHER_GOV

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Responsibility Role SPONSOR

Principal Investigators

Learn about the lead researchers overseeing the trial and their institutional affiliations.

Mehmet Yilmaz

Role: PRINCIPAL_INVESTIGATOR

Kocaeli City Hospital Anesthesiology and Reanimation

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

Kocaeli City Hospital

Kocaeli, , Turkey (Türkiye)

Site Status

Countries

Review the countries where the study has at least one active or historical site.

Turkey (Türkiye)

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

2023-31

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

Additional clinical trials that may be relevant based on similarity analysis.