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Comparison of Video-Light Intubating Stylet and Direct Laryngoscope for Nasotracheal Intubation in Patients Undergoing Elective Oral and Maxillofacial Surgery: Success Rate, Intubation Time, and Incidence of Epistaxis

Comparison of Video-Light Intubating Stylet and Direct Laryngoscope for Nasotracheal Intubation in Patients Undergoing Elective Oral and Maxillofacial Surgery: Success Rate, Intubation Time, and Incidence of Epistaxis

Status
Recruiting
Phases
Phase 1
Study type
Interventional
Source
TCTR
Registry ID
TCTR20260707005
Enrollment
302
Registered
2026-07-07
Start date
2026-07-05
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

Nasotracheal intubation in patients undergoing elective oral and maxillofacial surgery. Nasotracheal intubation Hemodynamic change Epistaxis Intubation time Video-Light Intubating Stylet Direct laryngoscope

Interventions

Use the DL for nasal intubation,Use the SL for nasal intubation
Experimental Procedure/Surgery,Active Comparator Procedure/Surgery
DL group,SL group

Sponsors

Maharat Nakhon Ratchasima Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: 1. Adults age 18-99 years 2. Scheduled for elective oral or maxillofacial surgery under general anesthesia with an indication for nasotracheal intubation 3. American Society of Anesthesiologists (ASA) physical status 1-3

Exclusion criteria

Exclusion criteria: 1. Basilar skull fracture 2. Severe maxillofacial fracture 3. Coagulopathy, current anticoagulant therapy, or any condition associated with an increased risk of significant epistaxis 4. Nasal obstruction caused by severe nasal stenosis or intranasal foreign bodies 5. Acute epiglottitis with a potential risk of complete airway obstruction during intubation 6. Patients at high risk of pulmonary aspiration

Design outcomes

Primary

MeasureTime frame
Intubation time From apply ETT into the nostril until remove device outside tube into the nostril until remove the device duration in second,success rate success within 3 times times

Secondary

MeasureTime frame
Incidence of epistaxis after finished nasotracheal intubation Grading severity of bleeding: bleeding score,Hemodynamic change Baseline, after induction, 3 and 5 minutes after intubation SBP , DBP, MAP, HR

Countries

Thailand

Contacts

Public ContactThidarat Ariyanuchitkul

Maharat Nakhon Ratchasima Hospital

arthidarat@gmail.com044235040

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 10, 2026