Clinical Trials Logo

Clinical Trial Summary

Design: Nasotracheal intubation is a standard blind procedure associated with various complications. Selection of the appropriate nostril is crucial in preventing most of these complications. The investigators aimed to evaluate the contribution of CBCT findings in selecting the proper nostril for nasotracheal intubation. Methods: This prospective observational study outlines the protocol for research conducted at the Selçuk University Faculty of Dentistry. Scope of the Research: The study encompasses patients undergoing dental surgery under general anesthesia at the Selçuk University Faculty of Dentistry. 1. Participant Selection: ASA I-II patients will be included in the study. Patients with structural abnormalities in the maxillo-mandibular anatomy, limited mouth opening, comorbidities such as rheumatoid arthritis, and a history of epistaxis will be excluded from the study. 2. Anesthesia Method: General anesthesia induction will be performed with intravenous (IV) propofol, IV rocuronium bromide, and IV fentanyl. Transition to nasotracheal intubation will follow adequate mask ventilation, and the preferred nostril will be determined through a simple occlusion test. 3. Data Collection: Demographic data, accompanying illnesses, medications used, and various parameters related to nasotracheal intubation will be recorded. The anesthetist performing nasotracheal intubation will be blinded to CBCT data, and the evaluation of data will be conducted jointly by the anesthetist and Radiology specialist after data collection from all patients is complete. 4. Exclusion Criteria: Unsuccessful nasotracheal intubation, difficult mask, and/or difficult intubation. 5. Implementation and Evaluation: Anesthesia procedures and CBCT evaluations will be carried out by experienced specialists. 6. The objective of this study is to evaluate the use of preoperative measurements of the nasal cavity from CBCT images in selecting the appropriate nostril for nasotracheal intubation under general anesthesia. The statistical tests to be employed are the chi-squared test and independent samples t-test.


Clinical Trial Description

The goal of this prospective observational study is the contribution of CBCT findings in selecting the proper nostril for nasotracheal intubation. The main question it aim to answer is: 1. Can pre-operative evaluations of participiants' nasal cavity by using CBCT aid anesthetists for selecting the appropriate nostril for nasotracheal intubation? The participants will be informed both through a written consent form, and verbally that they would be participating in the observational study, and that apart from routine procedures, no additional interventions would be performed. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06247969
Study type Observational
Source Selcuk University
Contact
Status Completed
Phase
Start date December 19, 2023
Completion date February 5, 2024

See also
  Status Clinical Trial Phase
Active, not recruiting NCT05717907 - Suction Catheter as a Guide for Nasotracheal Intubation Under General Anesthesia N/A
Completed NCT03653910 - Effect-site Concentration of Remifentanil for Double-lumen Tubes Intubation: Airtraq VS Macintosh Laryngoscope N/A
Recruiting NCT04190524 - Sonographic Assessment of Cricoid Pressure N/A
Completed NCT02359370 - The Effects of Lidocaine and Magnesium Sulphate on the Attenuation of the Hemodynamic Response to Tracheal Intubation Phase 4
Not yet recruiting NCT05036460 - Real-time Sonography in Detecting Inadvertent Esophageal Intubation Among Difficult Intubation Patients N/A
Completed NCT05502120 - A Comparison of Vie-Scope and Macintosh Blade Laryngoscopes in Morbidly Obese. N/A
Completed NCT03992950 - Effectiveness of Cricoid and Paratracheal Pressures for Occluding Esophagus N/A
Completed NCT05303948 - Evaluation of Two Positions for Free Floating Tracheal Intubation in Weightlessness N/A
Completed NCT03720093 - Exploratory Analysis of Pulmonary Microbiome in Intubated Patients
Recruiting NCT03031808 - Comparison of Two Induction Regimens Using Topical Lidocaine or Muscle Relaxant on Sore Throat and Hemodynamics Phase 4
Not yet recruiting NCT02918526 - Hemodynamic Study With PRAM of the Cardiovascular Response to the Positioning of the Extraglottic Device N/A
Completed NCT02364622 - The Effects of Flexible Intubating Stylet in the Accurate Placement of Double-lumen Endobronchial Tube N/A
Completed NCT05249738 - Tongue Edema Caused by Intubation Tube in Intensive Care Unit Patients
Terminated NCT03340207 - Novel Airway Device to Aid Endotracheal Intubations N/A
Completed NCT03842306 - End-tidal Oxygen Can Reliably Predict the Arterial Partial Pressure of Oxygen Among Emergency Department Patients
Recruiting NCT05782517 - I-gel vs. Endotracheal Intubation for Laparoscopic Gynaecological Procedures N/A
Recruiting NCT06085326 - Smart Checklist Implementation for Pediatric Tracheal Intubations in the ICU- Multicenter Study N/A
Active, not recruiting NCT06108271 - Innovative Endotracheal Tube Design Reduces Postoperative Laryngeal Injury N/A
Completed NCT05668299 - Determining the Appropriate Setting of an Automated Secretion Removal Technology (TrachFlush) N/A
Completed NCT04079387 - Effect of Endotracheal Tube Plus STYLET Versus Endotracheal Tube Alone N/A