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CTRI Number  CTRI/2025/06/088013 [Registered on: 02/06/2025] Trial Registered Prospectively
Last Modified On: 28/05/2025
Post Graduate Thesis  No 
Type of Trial  Interventional 
Type of Study   Surgical/Anesthesia 
Study Design  Randomized, Parallel Group Trial 
Public Title of Study   Comparing Two Breathing Methods to See Which Helps Premature Babies Recover Faster After Eye Surgery 
Scientific Title of Study   A prospective Randomized Comparative analysis between LMA vs ETT for Recovery time in Preterm infants for ROP eye surgeries 
Trial Acronym  nil 
Secondary IDs if Any  
Secondary ID  Identifier 
NIL  NIL 
 
Details of Principal Investigator or overall Trial Coordinator (multi-center study)  
Name  Dr Sushmita Bairagi 
Designation  Assistant Professor 
Affiliation  Department of anesthesia, AIIMS, Delhi 
Address  Room no. 431, Surgical block, Department of Anesthesia, AIIMS, New Delhi, 110029

South
DELHI
110029
India 
Phone  09953060597  
Fax    
Email  sushmita.bairagi91@gmail.com  
 
Details of Contact Person
Scientific Query
 
Name  Dr Sushmita Bairagi 
Designation  Assistant Professor 
Affiliation  Department of anesthesia, AIIMS, Delhi 
Address  Room no. 431, Surgical block, Department of Anesthesia, AIIMS, New Delhi, 110029

South
DELHI
110029
India 
Phone  09953060597  
Fax    
Email  sushmita.bairagi91@gmail.com  
 
Details of Contact Person
Public Query
 
Name  Dr Sushmita Bairagi 
Designation  Assistant Professor 
Affiliation  Department of anesthesia, AIIMS, Delhi 
Address  Room no. 431, Surgical block, Department of Anesthesia, AIIMS, New Delhi, 110029

South
DELHI
110029
India 
Phone  09953060597  
Fax    
Email  sushmita.bairagi91@gmail.com  
 
Source of Monetary or Material Support  
Department of Anesthesia, AIIMS, New Delhi,India, 110029 
 
Primary Sponsor  
Name  AIIMS New Delhi 
Address  Department of Anesthesia, AIIMS, New Delhi, India, 110029 
Type of Sponsor  Government 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 Sushmita Bairagi  AIIMS, New Delhi India  Operation theatre of Rajendra Prasad Centre, eye OT, Aiims, New delhi
South
DELHI 
09953060597

sushmita.bairagi91@gmail.com 
 
Details of Ethics Committee  
No of Ethics Committees= 1  
Name of Committee  Approval Status 
Institute Ethics Committee   Approved 
 
Regulatory Clearance Status from DCGI  
Status 
Not Applicable 
 
Health Condition / Problems Studied  
Health Type  Condition 
Patients  (1) ICD-10 Condition: H00-H59||Diseases of the eye and adnexa,  
 
Intervention / Comparator Agent  
Type  Name  Details 
Comparator Agent  ETT  The preterm infants undergoing ROP eye surgeries will undergo inhalation induction and muscle relaxant will be given for inserting the ETT into the trachea. controlled ventilation will be done and after the end of the surgery reversal of neuromuscular blockade will be done and recovery time will be checked till the baby is fully awake and ETT is removed. The total duration of intervention is from the time the ETT is inserted post induction till the ETT is removed after extubation(approximately 1 to 2 hours depending on the duration of surgery) 
Intervention  LMA  The preterm infants undergoing ROP eye surgeries under general anesthesia will undergo inhalation induction and no muscle relaxant will be given, LMA airway device will be inserted and patient will be under spontaneous ventilation. after the end of the surgery recovery from the anesthesia will be checked till the baby is fully awake and LMA is removed. The total duration of intervention is from the time LMA is inserted post induction till the LMA is removed after extubation (approximately 1 to 2 hours depending on the duration of surgery) 
 
Inclusion Criteria  
Age From  1.00 Day(s)
Age To  12.00 Month(s)
Gender  Both 
Details  1) Infants less than 1 year of age of either gender posted for any ROP intervention in the OT.
2) Patients belonging to the American Society of Anesthesiologists’ Physical Status Grade I, II, or III.
3) Guardians giving willful consent for the participation in the study
 
 
ExclusionCriteria 
Details  1) Patients with restricted mouth opening.
2) Patients with airway obstruction.
3) Patients with distorted airway.
4) Patients with history of stiff lungs, recent pneumonia.
5) Patients with history of recent upper respiratory tract infections.
 
 
Method of Generating Random Sequence   Computer generated randomization 
Method of Concealment   Sequentially numbered, sealed, opaque envelopes 
Blinding/Masking   Participant Blinded 
Primary Outcome  
Outcome  TimePoints 
To observe postoperative recovery time between laryngeal mask airway and ETT that is being used in infants presenting for ROP procedures.  Post extubation- 1 hrs, 2hrs, 3 hrs and 24 hrs post extubation 
 
Secondary Outcome  
Outcome  TimePoints 
To study this population in terms of
• Patient demography- birth weight, birth week, gender
• First pass success rate
• Duration of insertion
• Ease of insertion
• Number of attempts
• Airway adjunct used
• Desaturation, bradycardia during insertion
• Time for extubation
• Perioperative complications
• Transfer to NICU for mechanical ventilation
 
1) post induction (5,10,15,20 minutes)- number of attempts, ease of insertion, time taken for insertion
2) intraoperative duration(1 to 2 hrs)- any events , desaturation
3) post extubation( 15, 30,45 minutes )- time taken for extubation, requirement of mechanical ventilation 
 
Target Sample Size   Total Sample Size="40"
Sample Size from India="40" 
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)   01/08/2025 
Date of Study Completion (India) Applicable only for Completed/Terminated trials 
Date of First Enrollment (Global)  01/08/2025 
Date of Study Completion (Global) Applicable only for Completed/Terminated trials 
Estimated Duration of Trial   Years="1"
Months="0"
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 - NO
Brief Summary  

 This study was designed to compare the recovery time between LMA vs ETT in preterm babies undergoing ROP eye surgeries. In this study we want to establish which mode is safer as well as better for airway management in preterm babies. We hypothesize that LMA will have better recovery  time than ETT in preterm babies undergoing ROP eye surgeries. 

Primary Objective: To observe postoperative recovery time between laryngeal mask airway and ETT that is being used in  infants presenting for ROP procedures.

Secondary Objective: To study this population in terms of 1) Patient demography- birth weight, birth week, gender 2)First pass success rate 3) Duration of insertion 4) Ease of insertion 5)Number of attempts 6)Airway adjunct used 7)Desaturation, bradycardia during insertion 8)Time for extubation 9)Perioperative complication 10)Transfer to NICU for mechanical ventilation

 A total of 40 Preterm babies of less than 1 year of age of either gender belonging to ASA physical status I,II,III will be recruited after receiving the parents willful consent.  Patients will be randomly allocated to LMA group and ETT group of 20 each.

Randomization will be achieved using a computer-generated random number table with an allocation ratio of 1:1. Allocation concealment will be maintained using sequentially numbered sealed opaque envelopes. Envelopes will be prepared by an independent person not involved in the study. Each envelope will contain a number which will allocate the participant to either Endotracheal group (ET group1) and Laryngeal mask airway ( LMA Group 2). The allocation sequence will be accessed only when study data collection is complete or in any instance where unblinding of the study is thought to be essential in the provision of appropriate patient care. 

Forty patients will be randomly divided into two groups of twenty in each – Group 1 and Group 2 based on the intervention received.

Group 1 (ET group): Endotracheal intubation will be done ( n = 20). 

Group 2 (LMA group): Laryngeal mask airway will be inserted(n = 20). 

Upon arrival of the patient in the OR, an anaesthesiologist who is not involved in the study or in the care of the patient will open the sealed opaque envelope containing group allocation. The intubation or LMA insertion will be done according to the group allocation. The patient guardian will be unaware of the group allocation.

ANAESTHESIA TECHNIQUE

PREOPERATIVE : 

·       A detailed routine preoperative evaluation will be done one day prior as per standard practice on all selected patients.

·       The post conceptual age, birth weight, gender, recent weight , history of NICU stay, history of mechanical ventilation or oxygen therapy, any other significant history will be noted.

·       The patients will be carefully examined for breath holding spells and if present the duration of spells and associated cyanosis or bradycardia.

·        Adequate fasting will be maintained as per standard guidelines.

IN THE OPERATING ROOM :

·       After confirming adequate fasting, patients will be taken to operation theatre table and standard ASA monitors will be attached.

·        Operation theatre temperature will be kept warm to prevent hypothermia in babies.

·       Inhalational induction of anaesthesia will be done using 100% O2 and titrated doses of Sevoflurane and maintenance of anaesthesia will be done using 50% O2 in air and titrated doses of Sevoflurane to maintain minimum alveolar concentration (MAC) >1.

·       An appropriately sized intravenous cannula will be secured.

·       Administration of Injection Atracurium (0.2–0.5 mg/kg) will be given in ETT group whereas injection atracurium will be avoided in LMA group.

·       Weight appropriate supraglottic airway device and endotracheal tube will be selected based on manufacturer’s guidelines.

·       The type of LMA or ETT device use will be decided by the concerned anaesthesia consultant and surgeon. A senior anaesthetist experienced in paediatric cases will only insert the LMA/ ETT and confirm the placement. Successful insertion of LMA/ETT will be defined on confirming the ventilation with capnograph, chest rise, and acceptable leak without overtly increasing airway pressure.

·       If fail to ventilate or/and secure the airway, other rescue measures including endotracheal intubation, or awakening the patient can be attempted by the concerned anaesthetist depending upon the situation.

·       PSV mode of ventilation will be used in case of LMA targeting a tidal volume of 6-8 ml/kg and VCV /PCV mode of ventilation will be used in case of ETT insertion targeting a volume of 6-8 ml/kg body weight.

·       Maintenance of anaesthesia will be done with isoflurane and 50% O2 in air to target a MAC of 1.2.

·       Hemodynamic parameters will be noted.

·       All the patients will receive injection Paracetamol 10 mg/kg IV.

·       Reversal of neuromuscular blockade will be achieved by Neostigmine 70mcg/kg and Glycopyrrolate 10mcg/kg in patients of ETT group.

·       The LMA/ETT will be removed in an awake state and the patient will be observed for any complication in the neonatal intensive care unit (NICU).

·       The following parameters will be studied.

Parameters:

·       Success: Number of attempts needed to insert and secure the LMA/ETT with confirmed ventilation will be counted and noted.

·       The duration of insertion will be measured from picking up of LMA/ETT to the confirmation of LMA/ETT placement by two square wave patterns in the capnogram on the monitor.

·       The ease of insertion will be defined by objective criteria as mentioned in the Table 1.

 

 

Easy placement

Difficult placement

Time for insertion

<30sec

>30sec

First Attempt success rate

Success

Failure

Adjuncts or Manoeuvres

No

Yes

         Table1: Objective criteria for defining easy vs difficult placement of LMA/ETT

 

·       A difficult placement will be defined by the presence of any one criterion while an easy placement can only be defined by presence of all three criteria.

·       Any Incidence of desaturation or bradycardia requiring intervention/treatment, LMA/ETT displacement, re-insertion, and need for endotracheal intubation in LMA group and mechanical ventilation will be noted.

·        Recovery time (removal of LMA/ETT after end of surgery),Delayed extubation time>30 min, Desaturation With SpO2 < 95% ,Apnea >15 secs, bradycardia,manual ventilation and reintubation requirements, shifting patient intubated to NICU for mechanical ventilation will be noted.

·       Occurrence of any postoperative airway complication or evidence of airway trauma (i.e., presence of blood-tinged secretions on the dorsum of the LMA cuff) will be noted.

POSTOP:

·       Patients will be shifted to NICU for monitoring either extubated or intubated.

·       Any postoperative complications in NICU will be noted .

 DATA COLLECTION Data will be collected from the anesthetic chart and separate proforma which are specifically made for the intraoperative and postoperative monitoring of these patients. All documentation relating to the study will be stored in an anonymized case report file unique to each patient.

 

 
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