How neck measurements relate to airway checks to help in intubation
Official title: Correlation of Thyromental Distance And Mandibular Triangle Perpendicular Length With Incisor Vallecular Distance In Adult Pre-Surgical Patients: An Observational Study
Run by Sir Ganga Ram Hospital · NCT07668297 · Data updated 2026-11-12
This observational study tests whether the thyromental distance or the mandibular triangle length best predicts the distance to the incisor vallecula to aid choosing the right laryngoscope blade for intubation.
Quick facts
| Study type | Observational |
|---|---|
| Ages | 18 Years to 65 Years |
| Sex | All |
| Enrollment | 240 (estimated) |
| Sponsor | Sir Ganga Ram Hospital Academic / other |
| Locations | 1 site (New Delhi, National Capital Territory of Delhi) |
| Status | Recruiting |
| Started | June 25, 2026 |
| Main results expected | July 2027 |
| Study ends | August 2027 |
| Registry record updated | June 30, 2026 |
| Trial ID | NCT07668297 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Adults aged 18–65, both genders, ASA I–II, scheduled for elective surgery with controlled ventilation via orotracheal intubation, without anticipated airway difficulty or major dental issues.
✕Probably not a fit
Patients with anticipated difficult airways, significant dental abnormalities, or specific exclusions may not benefit from the correlations studied.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
In this observational study, researchers will measure thyromental distance (TMD) and mandibular triangle perpendicular length (MTPL) and compare them with incisor vallecula distance (IVD) to see which correlates more strongly. The goal is to develop a regression equation that can predict IVD from external measurements and help select the appropriate laryngoscope blade size. The study focuses on preoperative airway assessment to improve the safety and ease of direct laryngoscopy and intubation. Eligible participants are adults 18–65 undergoing elective surgery with controlled ventilation and no predicted difficult airway. Exclusions include significant dental issues, tobacco use, or an anticipated difficult airway.
Why it matters
Potential benefit: If successful, clinicians may better predict airway access and blade size from simple neck/dental measurements, potentially improving intubation safety.
How similar studies have gone: Previous airway assessment research has explored multiple predictors of laryngoscopy ease, with mixed results; this study aims to clarify which external measurements align best with vallecular distance.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria:
1. Age 18-65 years
2. Males and females
3. ASA (American Society of Anaesthesiologists) physical status I and II
4. Patients scheduled for elective surgery with controlled ventilation through orotracheal tube conduit
Exclusion Criteria:
1. Smokers (those who have smoked ≥100 cigarettes in their lifetime), chewing tobacco dependence or substance abuse
2. Submucous fibrosis: progressive fibrosis of the submucosal tissue leading to rigidity, relative trismus, and progressive decrease of mouth opening
3. Anticipated difficult airway
4. Patients requiring intubation with MacIntosh blade #4 or #5
5. Dental issues:
* missing tooth (upper/lower incisors, upper/lower premolar)
* crowded dentition: - irregular, misaligned, or overlapping teeth within a relatively small oral cavity
* presence of artificial teeth and/or dental implants
• Mandible/mandibular structure related issues:
* Retrognathia: - posterior displacement of the mandible relative to the maxilla or cranial base
* Prognathia: - anterior displacement of the mandible relative to the maxilla or cranial base
6. Emergency Surgery
7. Those requiring urgent rapid-sequence intubation due to the presence of a full-stomach status secondary to gastro-esophageal reflux disease, diaphragmatic hernia, among others.
8. Refusal to informed consent
Where it's running
-
Sir Ganga Ram Hospital
New Delhi, National Capital Territory of Delhi, India Recruiting
Study contacts
- Principal investigator: Amitabh Dutta, MD — Sir Ganga Ram Hospital, New Delhi-110060, India
- Study coordinator: Amitabh Dutta, MD
- Email: duttaamitabh@yahoo.co.in
- Phone: 00919810848064
Similar studies
Other studies for the same condition or treatment. Recruiting studies are listed first.
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Comparing stress response and intubation time with video versus direct laryngoscopes
This trial will test whether using a video laryngoscope instead of a direct laryngoscope gives steadier blood pressure and heart rate after intubation and changes how long intubation takes in adults having elective surgery.
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Nalbuphine versus fentanyl to reduce blood pressure and heart rate changes during laryngoscopy and intubation
This test sees if nalbuphine or fentanyl better prevents spikes in heart rate and blood pressure during intubation for people having cardiac surgery.
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Ultrasound measurement of airway anatomy in pregnant, preeclamptic, and nonpregnant women
This study will test whether simple ultrasound measurements of the throat can help predict difficult tracheal intubation in nonpregnant women, women with normal pregnancy, and women with preeclampsia having surgery under general anesthesia.
-
Timing of a single dexmedetomidine dose before laryngoscopy and intubation and its effect on stress response.
This trial will test whether giving one dose of dexmedetomidine earlier or closer to surgery can reduce the blood pressure and heart rate changes caused by laryngoscopy and intubation in adults aged 18–65 with ASA I–II.
-
Improving predictions for difficult airway management
This study is testing a new scoring system that uses both traditional checks and ultrasound images to better predict if adults will have a hard time with their airway during anesthesia.
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.