use of flexible scope along with video scope to enable passage of tube into windpipe
- Conditions
- Medical and Surgical,
- Registration Number
- CTRI/2023/01/048986
- Lead Sponsor
- JIPMER
- Brief Summary
After obtaining informed consent, patients presenting for elective or emergency surgery under general anaesthesia requiring tracheal intubation will be included in the study. Pre-anaesthetic and complete airway assessment will be done before surgery. After administering pre-medication and attaching standard ASA monitors, patients will be randomized into two groups - VLS and VLF. Anaesthesia will be induced using 2 mcg/Kg Fentanyl, 2 mg/Kg propofol and 0.1 mg/Kg vecuronium. Face mask ventilation will be done for three minutes after which the pillow placed under the patient’s head will be removed. The patient’s head will be stabilized using MILS manouvre applied by an assistant standing on the left side of patient’s head. In group VLS, intubation will be performed using C-Mac Video-laryngoscope. In group VLF, C- MAC video-laryngoscope will be inserted into the patient’s oral cavity by the primary anaesthesiologist which will the be handed over to an assisting anaesthesiologist after obtaining glottic view. The primary anaesthesiologist will then intubate using the flexible Tracheoscope ( aScope, Ambu Inc.,) which has been railroded with the Endotracheal tube. Time Taken to Intubate ( TTI) will be the time taken from the insertion of video-laryngoscope into the oral cavity until the appearance of 3 square capnogram waveforms. An attempt at intubation will be defined as the attempt to insert the video-laryngoscope blade into the oral cavity. Failed intubation will be defined as failure to intubate within 2 attempts
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- All
- Target Recruitment
- 158
- Patients scheduled for elective or emergency surgery requiring general anaesthesia with tracheal intubation 2) with ASA physical status classification 1 to 33 3) with modified Mallampati class 1 and 2.
- presence of predictors of difficult airway such as reduced mouth opening, restricted neck movements, BMI greater than 32 Kg/m2 and cervical spine pathology 2) patients requiring rapid sequence induction and intubation.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Time taken to intubate with Video-laryngoscopy Versus Video-laryngoscopy assisted Flexible Tracheoscope in patients with Manual In-Line Stabilization after induction of anaesthesia
- Secondary Outcome Measures
Name Time Method 1)Rate of first attempt successful intubation between the two groups 2) Incidence of complications such as desaturation, airway injury and bleeding and post-operative throat pain
Trial Locations
- Locations (1)
JIPMER
🇮🇳Pondicherry, PONDICHERRY, India
JIPMER🇮🇳Pondicherry, PONDICHERRY, IndiaVijayanthiPrincipal investigator7305625129everenchantingveena@gmail.com