Clinical Trials Logo

Clinical Trial Summary

The main objective of the proposed study is to clarify whether rotating a stylet-loaded endotracheal tube (ETT) 180 degrees prior to intubation will decrease the incidence of postoperative throat soreness, when compared to standard technique used in Standard of Care.


Clinical Trial Description

The researcher who is not blinded will randomize the patient to one of the three groups. Specific technique and procedure: - Investigators anesthesiologists assigned to perform the laryngoscopies will be limited to 6 with minimum 2 years of attending experiences to balance the variability. The results of inter-operator bias will be analyzed. - Endotracheal Tube (ETT) size will be: 7.0 for men and women unless there will be clinical indications to use a different size of Endotracheal Tube. - Stylet preparation: 75-degree angulation shaped preoperatively and ready for use - Blade for either McGrath, Macintosh, or direct laryngoscopy will be size 3 for women and size 4 for men. - Endotracheal Tube (ETT) 180: inserting endotracheal tube loaded with stylet, rotating the tube 180 degree clockwise as soon as the tube tip passes the vocal cords (glottis), and removing the stylet after the tube cuff passes through the vocal cords, which is a common practice. - Endotracheal Tube cuff filling air pressure will be 20 cmH2O. Inflation will be made using a hand-held airway pressure manometer. - Patient's data collection will be blinded for both patient and Investigators anesthesiologists assigned to perform the laryngoscopies - No medications including opiates, monitoring options, and medical decisions will be altered by the study. A member of the research team will follow-up (in person or phone-call) with each patient in the Post Anesthesia Care Unit (PACU) and 24+/- 3 hours after endotracheal tube removal to collect information regarding any symptoms of hoarseness or sore throat. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06231342
Study type Interventional
Source Ohio State University
Contact
Status Recruiting
Phase N/A
Start date May 31, 2023
Completion date May 31, 2027

See also
  Status Clinical Trial Phase
Withdrawn NCT02687100 - The Effects of Beclomethasone Upper the Endotracheal Cuff on the Occurrence of Sore Throat at Extubation Phase 4
Completed NCT03582787 - A Comparison of McGrath MAC Videolaryngoscopy and Macintosh Laryngoscopy for Orotracheal Intubation in Children With Torticollis N/A
Completed NCT03094754 - Excision Size and Location on the Postoperative Pain After Nevi Excision in Children
Recruiting NCT06380244 - Opioid-free Anesthesia as an Alternative to General Anesthesia in Abdominal Surgery N/A
Completed NCT05296668 - Cuffed Versus Uncuffed Tracheal Tubes in Neonates Undergoing Elective Surgery N/A
Completed NCT03396432 - The Videolaryngoscopy in Small Infants N/A
Not yet recruiting NCT06382831 - Opioid Free Versus Opioid Balanced Anesthesia in Ophthalmic Surgery Phase 2/Phase 3
Completed NCT02827123 - A Comparison of McGrath MAC Videolaryngoscopy and Macintosh Laryngoscopy for Orotracheal Intubation in Children N/A
Completed NCT03524586 - Comparison of the Cuff Pressure of a Taper-guard Cuffed Tube Between Ipsilateral and Contralateral Rotation of Head N/A
Completed NCT03155555 - Comparison of Carotid Peak Systolic Velocity Variation With Aortic Peak Systolic Velocity Variation in Pediatric Non-Cardiac Surgery