Dexmedetomidine infusion during laparoscopic bariatric surgery improves airway reflexes and hemodynamic outcome at tracheal extubation: A prospective, randomized, controlled study.
Not Applicable
Completed
- Registration Number
- CTRI/2011/091/000043
- Lead Sponsor
- Max Super Speciality Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 50
Inclusion Criteria
Patients with Body Mass Index (BMI) >35 kg/m2,
2. Patient either male or female with Age between 18-60 years posted for elective laparoscopic bariatric surgery.
Exclusion Criteria
Patients with severe COPD, heart block, bradycardia, hepatic impairment,
2. Allergy to dex and sulpha drugs, fentanyl, propofol and eggs,
3. Obvious difficult airway
4. Gastro-esophageal reflux.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method PRIMARY OUTCOME: Our primary Outcome will be to assess the incidence of cough at tracheal extubationTimepoint: Number of coughing episodes at emergence /extubation(coughing as a 5 point scale)
- Secondary Outcome Measures
Name Time Method SECONDARY OUTCOME: The secondary outcome will be to determine the awakening time, hemodynamic parameters and pain score at tracheal extubation.Timepoint: Richmond Agitation and Sedation Score (RASS)<br>Mean Arterial Pressure and heart rate at extubation<br>Pain Score