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CTRI Number  CTRI/2025/11/096874 [Registered on: 04/11/2025] Trial Registered Prospectively
Last Modified On: 03/11/2025
Post Graduate Thesis  Yes 
Type of Trial  Observational 
Type of Study   Cross Sectional Study 
Study Design  Other 
Public Title of Study   Physiological Airway Scoring System to predict Post Intubation Adverse effects 
Scientific Title of Study   Deriving a Physiological Airway Scoring System to predict post intubation adverse effects for patients undergoing endotracheal intubation in the Emergency Department. 
Trial Acronym  Nil 
Secondary IDs if Any  
Secondary ID  Identifier 
NIL  NIL 
 
Details of Principal Investigator or overall Trial Coordinator (multi-center study)  
Name  Ananya G Rao 
Designation  Post Graduate,Junior Resident 
Affiliation  Kasturba Medical College Manipal 
Address  Department of Emergency Medicine, Kasturba Medical College,Madav Nagar, Eshwar Nagar, Manipal, Karnataka 576104

Udupi
KARNATAKA
576104
India 
Phone  07760371333  
Fax    
Email  ananya2.kmcmpl2024@learner.manipal.edu  
 
Details of Contact Person
Scientific Query
 
Name  Dr Vimal Krishnan S 
Designation  Professor and Head of Department 
Affiliation  Kasturba Medical College Manipal 
Address  Department of Emergency Medicine,Kasturba Medical College,Madav Nagar, Eshwar Nagar, Manipal, Karnataka 576104

Udupi
KARNATAKA
576104
India 
Phone  9995389984  
Fax    
Email  vimal.krishnan@manipal.edu  
 
Details of Contact Person
Public Query
 
Name  Dr Vimal Krishnan S 
Designation  Professor and Head of Department 
Affiliation  Kasturba Medical College Manipal 
Address  Department of Emergency Medicine, Kasturba Medical College,Madav Nagar, Eshwar Nagar, Manipal, Karnataka 576104

Udupi
KARNATAKA
576104
India 
Phone  9995389984  
Fax    
Email  vimal.krishnan@manipal.edu  
 
Source of Monetary or Material Support  
Kasturba Medical College, Manipal Madav Nagar, Eshwar Nagar Manipal, Karnataka 576104 
 
Primary Sponsor  
Name  Dr Ananya G Rao 
Address  Madav Nagar, Eshwar Nagar, Manipal, Karnataka 576104 
Type of Sponsor  Other [Self] 
 
Details of Secondary Sponsor  
Name  Address 
nil  nil 
 
Countries of Recruitment     India  
Sites of Study  
No of Sites = 1  
Name of Principal Investigator  Name of Site  Site Address  Phone/Fax/Email 
Dr Ananya G Rao  Kasturba Medical College Manipal  Department of Emergency Medicine ,Madav Nagar, Eshwar Nagar, Manipal, Karnataka 576104
Udupi
KARNATAKA 
07760371333

ananya2.kmcmpl2024@learner.manipal.edu 
 
Details of Ethics Committee  
No of Ethics Committees= 1  
Name of Committee  Approval Status 
Institutional Ethics Committee- 2 (Student Resaerch)  Approved 
 
Regulatory Clearance Status from DCGI  
Status 
Not Applicable 
 
Health Condition / Problems Studied  
Health Type  Condition 
Patients  (1) ICD-10 Condition: O||Medical and Surgical,  
 
Intervention / Comparator Agent  
Type  Name  Details 
Intervention  Nil  Nil 
 
Inclusion Criteria  
Age From  18.00 Year(s)
Age To  99.00 Year(s)
Gender  Both 
Details  Adult patients (Age more than 18 years) requiring endotracheal intubation in the ED. 
 
ExclusionCriteria 
Details  1. Patients/Surrogate not providing consent
2. Patients undergoing intubation during cardiac arrest
3.Patients requiring Re-intubation
 
 
Method of Generating Random Sequence   Not Applicable 
Method of Concealment   Not Applicable 
Blinding/Masking   Not Applicable 
Primary Outcome  
Outcome  TimePoints 
a) Post intubation hypotension
b) Post intubation cardiac arrest
 
Up till 60 minutes post endotracheal intubation
 
 
Secondary Outcome  
Outcome  TimePoints 
nil   
 
Target Sample Size   Total Sample Size="327"
Sample Size from India="327" 
Final Enrollment numbers achieved (Total)= "Applicable only for Completed/Terminated trials"
Final Enrollment numbers achieved (India)="Applicable only for Completed/Terminated trials" 
Phase of Trial   N/A 
Date of First Enrollment (India)   16/11/2025 
Date of Study Completion (India) Applicable only for Completed/Terminated trials 
Date of First Enrollment (Global)  Date Missing 
Date of Study Completion (Global) Applicable only for Completed/Terminated trials 
Estimated Duration of Trial   Years="1"
Months="7"
Days="0" 
Recruitment Status of Trial (Global)   Not Yet Recruiting 
Recruitment Status of Trial (India)  Not Yet Recruiting 
Publication Details   N/A 
Individual Participant Data (IPD) Sharing Statement

Will individual participant data (IPD) be shared publicly (including data dictionaries)?  

Response - YES
  1. What data in particular will be shared?
    Response - Individual participant data that underlie the results reported in this article, after de-identification (text, tables, figures, and appendices).

  2. What additional supporting information will be shared?
    Response -  Study Protocol
    Response -  Statistical Analysis Plan
    Response - Informed Consent Form

  3. Who will be able to view these files?
    Response - Anyone

  4. For what types of analyses will this data be available?
    Response - To achieve aims in the approved proposal.

  5. By what mechanism will data be made available?
    Response - Proposals should be directed to [ananya2.kmcmpl2024@learner.manipal.edu].

  6. For how long will this data be available start date provided 24-12-2027 and end date provided 24-12-2029?
    Response - Beginning 3 months and ending 5 years following article publication.

  7. Any URL or additional information regarding plan/policy for sharing IPD? 
    Additional Information - nil
Brief Summary  
1. Title of the project:  
Deriving a Physiological Airway Scoring System to predict post intubation adverse effects for patients undergoing endotracheal intubation in the Emergency Department.
2. Type of Study: Prospective study- cross sectional study
3. Aims & objectives (hypotheses if applicable): 
AIM: To derive a physiologically difficult airway scoring system for identifying patients at risk of post-intubation adverse events using physiological parameters collected in the Emergency Department
OBJECTIVES:
•Primary Objective: 
 To derive a predictive scoring system for identifying patients at risk of post-intubation hypotension, cardiac arrest using key physiological parameters collected prospectively in the Emergency Department (ED).
•Secondary Objectives: 
Clinical profile of patients undergoing endotracheal intubation in the ED, and estimate the incidence of Post intubation hypotension and cardiac arrest
4. Justification for study (whether of national significance with rationale): 
Airway management is a critical aspect of emergency medicine that requires prompt and accurate decision-making to optimize patient outcomes. Airway management for critically ill and injured patients require quick decision making and active intervention with array of skills by physicians in the Emergency Department (ED). Although endotracheal intubation as part of airway management is a life- saving intervention, it carries risks, including post-intubation hypotension and cardiac arrest, which contribute significantly to patient morbidity and mortality in the Emergency Department (ED). Traditional airway triage systems often rely on anatomical variables, which may fail to identify patients at risk for these adverse events. Anatomical scoring systems usually predict the difficulty in the process of intubation rather than post intubation adverse effects. The current scoring systems like Simplified Airway Risk Index(SARI),MTAC Scoring, Wilson’s Score lack important physiological parameters. Post intubation adverse effects like hypotension and cardiac arrest constitute a significant risk for patients in the ED. Predicting post intubation adverse effects using a triage scoring system may potentially help emergency physicians for optimizing airway management in the ED. This study aims to derive an airway triage system that leverages objective physiological parameters to predict the risk of post-intubation hypotension and/or cardiac arrest (post-intubation adverse events), thereby improving airway decision-making and patient safety in the ED.
(Reference:
 Griesdale DEG, Bosma TL, Kurth T, Isac G, Chittock DR. Complications of endotracheal intubation in the critically ill. Intensive Care Med. 2008 Oct;34(10):1835-42.
Crawley S, Dalton A. Predicting the difficult airway. BJA Education. 2015 Oct;15(5):253-8.)
5. Departments involved: Department of Emergency Medicine, KMC Manipal, MAHE
6. Study period: November 2025-June 2027(19 months) 
7. Sample size: 
On the basis of study done by Dr Pranav Prakash ,Dr Jayaraj MB, Dr Nisarg,  assuming p=28.6%(Prevalence of Post intubation hypotension) with 95% Confidence Interval & allowable error, the sample size estimated is 327
(Reference-Prakash P, S N, Balakrishnan JM, Alli SD, S RG, Naik SR. Right ventricular dysfunction: a key predictor of post-intubation hypotension in the emergency department. Int J Emerg Med [Internet]. 2025;18(1):183.)

 
8. Materials and methods:
a) Inclusion and exclusion criteria: 
Inclusion Criteria: 
Adult patients(Age more than 18 years) requiring endotracheal intubation in the ED.
Exclusion Criteria: 
                1. Patients/Surrogate not providing consent
                2. Patients undergoing intubation during cardiac arrest
                3.Patients requiring Re-intubation


b) Statistical methods: Descriptive statistics such as Mean Standard Deviation, Median, Interquartile range will be used to summarize continuous variables. Categorical variables will be represented as percentages. Chi square test will be used test the association between the scores and post intubation complications. Univariate and multivariate logistic regression will be used to identify the determinants of Post intubation hypotension.ROC Curve will be used to determine the cutoffs for the scores- Physiological Airway Scoring System. P<0.05 will be considered to be statistically significant. Sensitivity, specificity, PPV will be used.

9. Detailed description of procedure / processes: Data will be prospectively collected from ED patients with potential airway compromise at the time of presentation to the ED. Variables will include demographics, vital signs (e.g., respiratory rate, oxygen saturation, heart rate, blood pressure), arterial blood gas values, laboratory values, Glasgow Coma Scale (GCS) scores, Safe apnea time, point of care ultrasound including echo (including TAPSE) and airway ultrasound variables, provisional diagnosis, human factors including experience of airway manager and other relevant clinical parameters. In addition, details of the airway management procedure, time to decision making(from the time patient arrives in ED to communication for consent), time to intubation/ securing the airway and the occurrence of post-intubation complications—specifically hypotension (e.g., a defined drop in blood pressure) and/or cardiac arrest—will be documented. Patient will be monitored for 60 minutes post intubation for adverse effects. Consent will be taken before the patient is intubated.

10. Outcome measures
a) Post intubation hypotension
b) Post intubation cardiac arrest
11. Potential risks and benefits: 
RISK-MINOR INCREASE OVER MINIMAL RISK
BENEFIT-The results of the study will help us identify post intubation adverse effects in future patients. This will help us in optimizing airway management in the ED
12. Ethical considerations and methods to address issues:  IEC clearance. 

Institutional Review Board (IRB)/CTRI approval will be obtained before data collection.
Informed consent will be obtained from all participants/ surrogates.
Patient confidentiality and data security will be maintained in accordance with ethical guidelines.
 
13. Budget (give details) and proposed funding source: (remove the table if not required. If more rows are required, you can add.)
Sl.No Details Justification Funding agency INR
1. Self funded Stationary Self                       3000
 
14.Review of literature-
Emergency airway management has evolved from being purely anatomical to a comprehensive, physiology-based approach that accounts for the patient’s physiological state, potential complications, contextual factors, and human elements.
Early studies (Mort, 2007) documented the high incidence of complications during endotracheal intubation (ETI), including post-intubation hypotension (PIH), hypoxemia, aspiration, and trauma. These findings emphasized the need for hemodynamic optimization and first-pass success to reduce risk.
Griesdale et al. (2008) reinforced these findings, reporting a 28% complication rate in ICU intubations, with higher risk in sicker patients and repeated attempts.
A major conceptual shift occurred with the introduction of the “physiologically difficult airway” by Heffner et al. (2013) and Mosier et al. (2015), who highlighted conditions like hypoxemia, hypotension, acidosis, and right ventricular failure as key predictors of adverse events. These studies emphasized pre-intubation physiological stabilization to prevent complications such as cardiac arrest.
Subsequent research deepened this physiological focus:
Vaporidi et al. (2020) described the impact of respiratory drive and patient–ventilator interactions on outcomes.
Mann et al. (2021) showed that even anatomical differences, such as smaller airways in females, influence respiratory physiology.
Sakles et al. (2017) demonstrated that advanced techniques like video laryngoscopy and neuromuscular blockade improve first-pass success and safety in the ED.
Kuzmack et al. (2018) introduced the HEAVEN criteria, integrating both anatomical and physiological risk factors for predicting difficult airways.
Crawley and Dalton (2015) advocated for a multifactorial assessment approach using history, examination, and various predictive tools.
Huitink (2024) proposed the “Airway Triage” concept, which replaces the narrow “difficult airway” idea with a holistic framework considering physiology, context, and human factors.
Modern emergency airway management emphasizes holistic assessment — integrating anatomical, physiological, and contextual factors — to anticipate and mitigate complications. The shift from “difficult airway” to “Airway Triage” represents a paradigm aimed at improving safety, standardizing practice, and reducing post-intubation adverse events in critically ill patients.

 


 
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