CTRI/2017/12/011040
Not Yet Recruiting
N/A
A prospective interventional study to detect the efficacy of bronchial cuff pressuremonitoring to detect the displacement of lung isolation device during elective thoracic surgeries.
Overview
- Phase
- N/A
- Intervention
- Not specified
- Conditions
- Not specified
- Sponsor
- Tata Memorial Hospital
- Status
- Not Yet Recruiting
- Last Updated
- 4 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •All adult ( \>18 years) patients undergoing thoracic surgeries requiring lung isolation.
Exclusion Criteria
- •Pediatric patients
- •Emergency surgeries
- •Patients with known anatomical anomaly (known anatomical variation/ endobronchial mass/ Broncho pleural fistula) in trachea and bronchus.
- •Patients with risk of contamination (blood/ secretions/pus) across the lungs. E.g. Patients with hemoptysis, infective lung conditions communicating with bronchus etc.
- •Patients with lung isolation devicesplaced in right main bronchus.
Outcomes
Primary Outcomes
Not specified
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