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Clinical Trials/CTRI/2017/12/011040
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.

Tata Memorial Hospital0 sites0 target enrollmentTBD

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.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
4 years ago
Study Type
Interventional

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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