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Endotracheal Tube (ETT) 180: Stylet-loaded Endotracheal Tube Rotation Before Insertion

Endotracheal Tube (ETT) 180: Stylet-loaded Endotracheal Tube Rotation Before Insertion to Decrease the Risk of Postoperative Sore Throat: a Randomized Double-Blind Prospective Trial.

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06231342
Enrollment
357
Registered
2024-01-30
Start date
2023-05-31
Completion date
2027-05-31
Last updated
2026-04-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Anesthesia, Endotracheal

Brief 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.

Detailed 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.

Interventions

DEVICEDirect Laryngoscope (DL)

DL allows visualization of the larynx. It is used during general anesthesia, for surgical procedures of the larynx, and during resuscitation.

DEVICEVideo laryngoscope (VL)

VL facilitates intubation while allowing clinicians to share and record real-time high-resolution images and video.

PROCEDUREEndotracheal Tube (ETT) 180

A novel maneuver has been described to decrease the insult from stylet named Endotracheal Tube (ETT) 180; a clockwise rotation of the stylet-loaded Endotracheal Tube (ETT) 180 degrees on its axis right after the tip of Endotracheal Tube (ETT) passes the patient's vocal cords (glottis) before fully inserting the Endotracheal Tube (ETT) and then, pulling the stylet out. This maneuverer allows the stylet to match the posterior angulation of the trachea.

Sponsors

Ohio State University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
DOUBLE (Subject, Outcomes Assessor)

Masking description

Subjects and research personnel assessing subjects during follow-ups will be blinded throughout the study. Only the clinicians inside the operative room will be unblinded.

Intervention model description

A prospective double-blinded randomized trial

Eligibility

Sex/Gender
ALL
Age
18 Years to 90 Years
Healthy volunteers
No

Inclusion criteria

* ASA I - III * Ambulatory patients undergoing general anesthesia with an Endotracheal Tube (ETT) placement * Admitted patients undergoing general anesthesia an Endotracheal Tube (ETT) placement * Age \> 18 and \< 90 years old * BMI \< 50

Exclusion criteria

* Age \< 18 years old or age \> 90 years old * Pregnant women * Prisoners * Any surgery involving the pharynx, larynx, vocal cords, trachea that will create confounding factors related to postoperative sore throat * History of difficult airway * Critically ill patients requiring intensive care

Design outcomes

Primary

MeasureTime frameDescription
Incidence of postoperative sore throat24 hours after Endotracheal Tube (ETT) placementTo assess the differences in incidence of postoperative sore throat after intubation between the conventional technique and ETT 180 rotation of the ETT.

Secondary

MeasureTime frameDescription
Incidence of hoarseness/sore throat24 hours after Endotracheal Tube (ETT) placementTo assess the incidence of hoarseness/sore throat
Severity of hoarseness/sore throat24 hours after Endotracheal Tube (ETT) placementTo assess the severity of hoarseness/sore throat using a 0-3-point scale (units), where 0 = no hoarneseness/sore throat at all and and 3 = very bad hoarseness/sore throat sensation.
Incidence of analgesic medication requirements to treat sore throat.24 hours after Endotracheal Tube (ETT) placementTo assess the incidence of analgesic medication to treat sore throat sensation.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Apr 30, 2026