Prospective randomized controlled trial for qualitative comparison between the double lumen tube and the bronchus blocker EZ-blocker Endobronchial Blocker® (Teleflex Life Sciences) for one-lung ventilation during thoracic surgery

Phase 4

• Conditions: process times, quality of lung lung collapse; T88.4; Failed or difficult intubation

• Registration Number: DRKS00014816
• Lead Sponsor: Klinik für Anästhesie und Intensivmedizin, Universitätsklinikum Gießen und Marburg, Standort Marburg

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2018-06-07
• Study Completion: 2020-03-01
• Last Update Posted: 19 August 2024

Recruitment & Eligibility

• Status: Complete
• Sex: All
• Target Recruitment: 80

Inclusion Criteria

Patients undergoing elective thoracic surgery and for what DLT-intubation for one-lung ventilation is required

Exclusion Criteria

- patients who did not consent to the study

- pregnant patients

- patients who have not reached the age of 18 years

- patients with indications for so-called rapid sequence induction

- patients who have a contraindication to one-lung ventilation

- patients with severe cervical spine movement restriction, e.g. ankylosing spondylitis

- patients who are not capable to consent

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
The primary endpoint is time to achieve lungseparation