NC/TMD Ratio as a Difficult Airway Predictor in Obese Patients

February 20, 2023 updated by: Mahnoor Shabbir, KRL Hospital, Islamabad

Neck Circumference to Thyromental Distance Ratio as a Reliable Indicator for Predicting Difficult Intubation in Obese Patients for Elective Surgery Under General Anesthesia

To assess accuracy of NC/TM distance ratio in terms of sensitivity, specificity, negative predictive value (NPV) and positive predictive value (PPV) for predicting difficult intubation in obese patient with Intubation difficulty score (IDS) as gold standard.

Study Overview

Status

Recruiting

Detailed Description

At Preanaesthesia clinic patients , neck circumference to Thyromental distance ratios of obese patients with BMI >30Kg/m2 will be calculated and patients will be divided into two groups on the basis of Nc/TMD ratio as anticipated easy intubation ( NC/TMD<5) And anticipated difficult intubation ( NC/TMD ≥5).

Intra-operatively, patients Intubation difficulty scale score will calculated and the data obtained from IDS score will be compared with NC/TMD ratio as a predictor of difficult Intubation and diagnostic accuracy of NC/TMD as a reliable indicator of difficult intubation in obese patients will be calculated by statistical analysis.

Study Type

Observational

Enrollment (Anticipated)

220

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Locations

    • ICT
      • Islamabad, ICT, Pakistan, 44090
        • Recruiting
        • KRL Hospital
        • Contact:
        • Principal Investigator:
          • Mahnoor Shabbir, MBBS

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years to 65 years (Adult, Older Adult)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

Obese patients (BMI ≥30Kg/m2) of all genders, between age of 18 to 65 years, belonging to ASA class I-III, Undergoing elective surgery under general anesthesia

Description

Inclusion Criteria:

  1. ASA physical status I to III
  2. Body Mass Index (BMI) of 30kg/m2 or more
  3. age 18-65 years

Exclusion Criteria:

  1. non consenting
  2. ASA class greater than III,
  3. patients undergoing general anesthesia without tracheal intubation or under regional anesthesia,
  4. patients with upper airway pathology such as maxillofacial fractures, upper airway tumors or cervical spine fracture, obstetric patients, refusal of the patient, previous head and neck surgery or radiotherapy.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

Cohorts and Interventions

Group / Cohort
Group A (predicted easy intubation)
Group A labelled as predicted easy intubation on the basis of NC/TM distance ratio <5
Group B (predicted difficult intubation)
Group B labelled as predicted Difficult intubation on the basis of NC/TM distance ratio ≥ 5

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Predictability of difficult airway
Time Frame: During anaesthesia induction
At the preanaesthetic examination neck circumference to thyromental distance ratio will be caculated in obese patients with BMI ≥ 30KG/m2 and the predictability of difficult airway will be evaluated by statistical analysis
During anaesthesia induction

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Mahnoor Shabbir, KrlH Islamabad

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

October 21, 2021

Primary Completion (Anticipated)

February 21, 2023

Study Completion (Anticipated)

February 21, 2023

Study Registration Dates

First Submitted

February 9, 2023

First Submitted That Met QC Criteria

February 9, 2023

First Posted (Actual)

February 21, 2023

Study Record Updates

Last Update Posted (Estimate)

February 23, 2023

Last Update Submitted That Met QC Criteria

February 20, 2023

Last Verified

February 1, 2023

More Information

Terms related to this study

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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