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CTRI Number  CTRI/2021/06/034159 [Registered on: 10/06/2021] Trial Registered Prospectively
Last Modified On: 10/07/2025
Post Graduate Thesis  No 
Type of Trial  Interventional 
Type of Study   Surgical/Anesthesia 
Study Design  Randomized, Parallel Group Trial 
Public Title of Study   A clinical trial comparing the efficacy of video laryngoscope with direct laryngoscope for placing an tracheal (wind pipe) tube in patients undergoing general anesthesia 
Scientific Title of Study   A randomised controlled study comparing the efficacy of video-laryngoscope versus direct layngocope with Macintosh blade in patients undergoing general anesthesia 
Trial Acronym   
Secondary IDs if Any  
Secondary ID  Identifier 
NIL  NIL 
 
Details of Principal Investigator or overall Trial Coordinator (multi-center study)  
Name  Dr Sindhu J 
Designation  Senior Resident 
Affiliation  Sri Devaraj Urs Academy of Higher Education and Reseach 
Address  Department of Anaesthesiology,Sri Devaraj Urs Academy of Higher Education and Research, PO box No. 62, Tamaka, Kolar, Karnataka, India

Kolar
KARNATAKA
563101
India 
Phone  9353457097  
Fax    
Email  sindhuvikram@hotmail.com  
 
Details of Contact Person
Scientific Query
 
Name  Dr Threja CK 
Designation  Associate Professor 
Affiliation  Sri Devaraj Urs Academy of Higher Education and Reseach 
Address  Department of Anaesthesiology,Sri Devaraj Urs Academy of Higher Education and Research, PO box No. 62, Tamaka, Kolar, Karnataka, India

Kolar
KARNATAKA
563101
India 
Phone  9845347909  
Fax    
Email  drthrejack@gmail.com  
 
Details of Contact Person
Public Query
 
Name  Dr Threja CK 
Designation  Associate Professor 
Affiliation  Sri Devaraj Urs Academy of Higher Education and Reseach 
Address  Department of Anaesthesiology,Sri Devaraj Urs Academy of Higher Education and Research, PO box No. 62, Tamaka, Kolar, Karnataka, India

Kolar
KARNATAKA
563101
India 
Phone  9845347909  
Fax    
Email  drthrejack@gmail.com  
 
Source of Monetary or Material Support  
University Research Grants, Sri Devaraj Urs Academy of Higher Education and Research.  
 
Primary Sponsor  
Name  Sri Devaraj Urs Academy of Higher Education and Research 
Address  Sri Devaraj Urs Academy of Higher Education and Research, PO box No. 62, Tamaka, Kolar, Karnataka, India 
Type of Sponsor  Private medical college 
 
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 Threja CK  Major OT, RL Jalappa Hospital, attached to Sri Devaraj Urs Academy of Higher Education and Research  Sri Devaraj Urs Academy of Higher Education and Research, PO Box no. 62,Tamaka, Kolar 563101
Kolar
KARNATAKA 
9845347909

drthrejack@gmail.com 
 
Details of Ethics Committee  
No of Ethics Committees= 1  
Name of Committee  Approval Status 
Central Ethics Committee, SDUAHER, Kolar  Approved 
 
Regulatory Clearance Status from DCGI  
Status 
Not Applicable 
 
Health Condition / Problems Studied  
Health Type  Condition 
Healthy Human Volunteers  Methods of endotracheal Intubation for providing general anaesthesia 
Patients  (1) ICD-10 Condition: O||Medical and Surgical,  
 
Intervention / Comparator Agent  
Type  Name  Details 
Comparator Agent  Direct Laryngoscopy  Direct Laryngoscopy will be done with Macintosh Blade which is the standard for endotracheal intubation in adults 
Intervention  Videolaryngoscopy  Manufacturer: Anesthetics India Private Limited. 
 
Inclusion Criteria  
Age From  18.00 Year(s)
Age To  50.00 Year(s)
Gender  Both 
Details  Patients accepted for Anaesthesia under ASA grade 1 and 2 
 
ExclusionCriteria 
Details  1.Patients with a Modified Mallapatti scoring of Grade 3 and Grade 4
2.Patients with restricted neck mobility
3.Patients with decreased inter- incisor gap (18-30 mm)
4.Patient refusal
 
 
Method of Generating Random Sequence   Permuted block randomization, fixed 
Method of Concealment   Sequentially numbered, sealed, opaque envelopes 
Blinding/Masking   Participant Blinded 
Primary Outcome  
Outcome  TimePoints 
To compare the following parameters with video laryngoscope and direct laryngoscope
1.Glottic view
2.Time for intubation in seconds 
15 minutes 
 
Secondary Outcome  
Outcome  TimePoints 
To compare the following parameters with video laryngoscope and direct laryngoscope

1. Number of intubation attempts
2. Stress response to intubation
3. Optimization maneuvers required to intubate
4. Complications such as mucosal trauma and bleeding 
15 minutes 
 
Target Sample Size   Total Sample Size="80"
Sample Size from India="80" 
Final Enrollment numbers achieved (Total)= "80"
Final Enrollment numbers achieved (India)="80" 
Phase of Trial   N/A 
Date of First Enrollment (India)   01/07/2021 
Date of Study Completion (India) 31/03/2022 
Date of First Enrollment (Global)  Date Missing 
Date of Study Completion (Global) 31/03/2022 
Estimated Duration of Trial   Years="1"
Months="6"
Days="0" 
Recruitment Status of Trial (Global)
Modification(s)  
Not Applicable 
Recruitment Status of Trial (India)  Completed 
Publication Details
Modification(s)  
Published 
Individual Participant Data (IPD) Sharing Statement

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

Response - NO
Brief Summary
Modification(s)  


A randomised controlled study comparing the efficacy of  video - laryngoscope  versus  direct laryngoscope with Macintosh blade in patients undergoing general anesthesia


Endotracheal intubation is an important skill of an anesthetist for securing the airway. It is a lifesaving procedure both in the ICU and operation theater. With the advancement in surgical procedures, there is an increasing incidence of patients presenting with more number of co-morbidities who are posted for surgery. This includes an increasing number of patients with difficult airway. The incidence of difficult laryngoscopy and intubation in Indian population is around 9.7% and 4.5% respectively 1.

 

The ASA defines difficult airway as a clinical situation in which a conventionally trained anesthesiologist experiences difficulty with facemask ventilation of the airway, difficulty with tracheal intubation or both2. Anesthesiologists have been constantly making efforts to develop skills and tools to manage difficult airway.

 

Video laryngoscopes are emerging as an important tool for the management of difficult airway. The ASA (American Society of Anesthesiology) suggests video laryngoscopy as an initial approach in case of a predicted difficult airway and as an alternative approach during the second attempt at intubation in an unanticipated difficult airway2. They can be used in cases with decreased mouth opening3, 4 and restricted cervical spine movements5,6. These are unique advantages of video laryngoscopes over conventional laryngoscopy. 

 

The demographics of the patients coming to our institution will benefit from this tool. We have patients being admitted under head & neck onco-surgery who have oral malignancies and decreased mouth opening. There are also a considerable number of road traffic accident patients with cervical spine injuries.

Hence, proficiency of use of video laryngoscopes in patients with a normal airway can help us put it use in the emergency situations7, where it can be life- saving.

 

a.  Design: A randomized controlled trial.

 b.  Total number of study subjects: The sample size is based on time to intubation, as reported in a similar study by Reena et al 10.The sample includes patients in the age group of 18 – 50 years. The study reported an average variance estimate of 12.52 seconds, with a 90% power and an error of 1%. To detect a difference of 28% in time for intubation, an estimated sample size will be 35 per group. Expecting a non - compliance, the final sample size is 35 + 5, which is equal to 40 in each group. The sample size was calculated using OpenEpi version 3.01

 

c.   Mode of selection:

After approval from the central ethical committee, an informed written consent will be obtained from all patients before including them in the study. The subjects for the 2 groups will be chosen using block randomization technique, with a block size of 4.  

 

Anesthetists who have a minimum experience of 100 intubations with Macintosh blade and 30 intubations with  video laryngoscope will perform the laryngoscopy. 

 

Group L: Patients will undergo a direct laryngoscopy with Macintosh Laryngoscope. The Cormack – Lehane Grading and POGO scoring in sniffing position will be assessed. This will befollowed by stylet- assisted endotracheal intubation.

 

Group K: Patients will undergo video laryngoscopy ( by Anesthetics India Private Ltd.) with Videolaryngoscope. Endotracheal intubation assisted by a stylet will be done after assessing the Cormack – Lehane Grading and POGO scoring in sniffing position.

 

The primary outcome measures will be assessment of grade of glottic view and time to intubation. 

 

 

c.   Inclusion Criteria: 

1.      Adults aged between 18 to 50 years, 

2.      ASA grade I and II planned for General Anesthesia

 

d.  Exclusion Criteria:

1.      Patient refusal

2.      Patients with modified Mallampatti scoring of Grade 3 and 4

3.      Patients with restricted neck mobility

4.      Patients with decreased inter- incisor gap (18 mm-30 mm) 

 

Data will be entered into Microsoft excel data sheet and will be analyzed using SPSS 22 version software. Categorical data will be represented in the form of Frequencies and proportions. Continuous data will be represented as mean and standard deviation. Chi-square will be the test of significance. Independent t test will be the test of significance to identify the mean difference between two groups. P value <0.05 will be considered as statistically significant 



 
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