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
|
|
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
|
|
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 anï¡ 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
|