Comparison of health status outcome in people undergoing lung surgery using special tube used for aerating one lung under two different types of anesthesia drugs.
Not Applicable
- Conditions
- Health Condition 1: O- Medical and Surgical
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Adults aged 20-65 years
ASA-PS I-III
Patients undergoing elective thoracotomy for lung resection with OLV
Exclusion Criteria
Patients with severe cardiac disease, hepatic or renal dysfunction
patients with a prior allergic history of any study drug
Patients taking sedative, opioid or sleep aid drugs
Patients with Psychiatric or neurological disorder
BMI >30 kg/m2
Pregnancy
History of pneumonectomy or lung volume reduction surgery
patients with severe systemic infections
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To compare EQ5D3L scores 3 months after surgery in patients undergoing lung resection under one lung ventilation between patients administered inhalation & intravenous anesthesiaTimepoint: Outcome will be analysed after collection of data for the requisite sample size
- Secondary Outcome Measures
Name Time Method 1. To compare the composite of Neurological, Cardiovascular & Pulmonary complications <br/ ><br>2. To compare the length of hospital stay <br/ ><br>3. To compare the need of mechanical Ventilation support required postoperatively <br/ ><br>4. To compare the number and types of rescue strategy adopted intraoperatively: PEEP/CPAP/High FiO2/Inotropes support/ Crossover to other strategyTimepoint: Outcome will be analysed after collection of data for the requisite sample size