A study to check the efficacy of right-sided double lumen tube in surgeries of thoracic region.
Not Applicable
- Conditions
- Health Condition 1: C349- Malignant neoplasm of unspecifiedpart of bronchus or lung
- Registration Number
- CTRI/2023/03/050319
- Lead Sponsor
- Tata Memorial Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Open to Recruitment
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
All adult patients undergoing one-lung ventilation using right-sided DLTs placed in the right main bronchus.
Exclusion Criteria
1.Emergency surgery
2.Patient < 18 years of age
3.Endobronchial masses inside the trachea, right mainstem bronchus (RMB), or bronchus intermedius (BI)
4.Radiological evidence of compression or deviation of the trachea, RMB, or BI.
5.Patients planned for right pneumonectomy/right bronchial sleeve surgery or right bronchotomy.
6.Patient with anatomical variation in the trachea e.g. Pig Bronchus
7.Patients with a height of less than 150 cm
8.Patients with tracheostomy or anticipated difficult airway
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The incidence of intra-operative hypoxia associated with the use of Right-sided double lumen tubeTimepoint: at 30 minutes, 60 minutes, 90 minutes, and 120 minutes after the beginning of one-lung ventilation.
- Secondary Outcome Measures
Name Time Method the time taken for the insertion of RDLT, number of attempts of intubation, rate of first attempt success, and rate of dislodgement of RDLTTimepoint: at 30 minutes, 60 minutes, 90 minutes, and 120 minutes after the beginning of one-lung ventilation.