A comparative study in nasotracheal fiberoptic intubation under conventional method v/s intravenous dexmedetomidine
Not Applicable
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2019/02/017751
- Lead Sponsor
- IMS BH
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Open to Recruitment
- Sex
- Not specified
- Target Recruitment
- 50
Inclusion Criteria
Patients belonging to ASA I and ASA II .
Patients undergoing GA with awake fiberoptic intubation in elective oropharyngeal , maxillo facial , mandibular surgeries , and general surgeries with difficult intubation.
Exclusion Criteria
head trauma, suspected base of skull fractures, nasal mass, allergy to local anaesthesia, pregnancy, infection at the local site
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method haemodynamic stability ( HR , SBP,DBP )Timepoint: 0,1,3,5,10,15,20 min
- Secondary Outcome Measures
Name Time Method vocal cord visibility, intubating conditions,duration of intubation, sedation using ramsay sedation score, patient comfort based on memory and recall.Timepoint: 0,1,3 min.