None listed
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1. Age between 18 65 years 2. American society of anesthesia classification physical status I and II 3. Body mass index BMI less than 30 kg/m 4. Mallampati Grade I or II, patients withouit a difficult airway 5. Patients who provide written informed consent
Exclusion criteria
Exclusion criteria: 1. patient refusal 2. Syndromic patients or those with congenital craniofacial or airway abnormalities 3. History of previous head and neck surgery 4. Anticipated difficult airway like mouth opening less than 1.5 cm, restricted neck movements. 5. Coagulopathy or bleeding disorders Known allergy to local anesthetics
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To compare the total intubation time (TIT) between the cuff inflation technique and the non cuff inflated technique under video laryngoscopy as a measure of procedural ease.Timepoint: T1- the total time taken to pass te he endotracheal tube from nose till it is visualised in the oropharynx t2- time taken to pass the tube from the oropharynx to the glottis between the vocal cords | — |
Secondary
| Measure | Time frame |
|---|---|
| 1. To compare the success rate and number of attempts required for nasotracheal intubation between both groups. 2. To objectively assess and compare the intubation difficulty using the Intubation Difficulty Scale (IDS). 3. To evaluate the need for adjuncts or alternative techniques such as Magill s forceps or bougie. 4. To assess the incidence of intraoperative trauma, including nasal bleeding, mucosal injury, or cuff rupture. 5. To compare post-extubation complications, such as sore throat, hoarseness, and pain on swallowing, between both groups. Timepoint: | — |
Countries
India
Contacts
Nizams institute of medical sciences