A clinical trial to study two drug regimens, dexmedetomidine and propofol-fentanyl combination sedation for a procedure, awake fiberoptic nasotracheal intubatio
Not Applicable
Completed
- Conditions
- Health Condition 1: null- Difficult Airway
- Registration Number
- CTRI/2018/01/011417
- Lead Sponsor
- Dr Radha M
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 60
Inclusion Criteria
1.ASA grade 1 to 3
2.Patients scheduled for elective awake fiberoptic intubation.
Exclusion Criteria
1.Baseline heart rate <60/min,any type of atrioventricular block on the ECG,heart failure
2.Emergency surgery,Pregnancy
Liver cirrhosis
3.Thrombocytopenia or coagulopathy contraindicating nasal intubation.
4.Known alcoholic or drug abusers,allergy to the drugs involved in the study
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Intubation scores,patient tolerance scores,airway obstruction scores during awake fiberoptic intubationTimepoint: one year fourmonths
- Secondary Outcome Measures
Name Time Method Ramsay sedation scale during AFOI,number of rescue midazolam requirement and haemodynamicsTimepoint: over one year four months