CompletedNot Applicable

Comparison of Airway Management With Bronchial Blocker and Double-Lumen Tube in Single-Lung Ventilation

Turkey (Türkiye)66 participantsStarted 2024-04-17

Plain-language summary

In this study, the primary aim is to compare the impact of using a double-lumen tube and bronchial blocker for single-lung ventilation in patients undergoing minimal invasive cardiac surgeries on postoperative pulmonary functions. Secondary objectives include the comparison of application duration, success in lung collapse, and the number of repositioning attempts for both techniques.

Who can participate

Age range18 Years

SexALL

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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * Patients planned for on-pump minimal invasive cardiac surgical procedures requiring single-lung ventilation * Female and male patients aged 18 and above * Patients with ASA scores of 1-2-3 * Patients with signed informed consent to participate in the study * Patients with a Body Mass Index (BMI) less than 40 Exclusion Criteria: * Emergency surgeries * Patients with ASA scores greater than 3 * Advanced-stage organ (heart, kidney, liver, lung) failure * Advanced lung diseases (COPD, FEV1\<50%, restrictive lung diseases, history of chest surgery, Pulmonary Hypertension, PAB\>30mmHg) * Patients with anticipated difficult intubation * Pregnant individuals * Patients with a BMI greater than 40 * Patients lacking the ability to read, understand, sign the informed consent form, and those who do not wish to participate in the study

What they're measuring

Comparison of Postoperative Pulmonary Complications in Patient Groups Undergoing Single-Lung Ventilation with Double-Lumen Tube and Bronchial Blocker

Timeframe: Postoperative 7 days

Trial details

NCT IDNCT06299735

SponsorAnkara City Hospital Bilkent

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2024-12-31