Flow-Controlled Ventilation to Improve Postoperative Pulmonary Outcome After Thoracic Surgery

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorCantonal Hospital of St. Gallen

About this trial

In an international multicenter randomized clinical pilot trial, intraoperative flow-controlled ventilation (FCV) will be compared with volume-controlled ventilation (VCV) in patients scheduled for (open, video- or robot-assisted) thoracic surgery with one-lung ventilation (OLV). This pilot trial is designed to test the feasibility and safety of FCV during all phases of intraoperative ventilation, and in particular during OLV, and to inform the design of a future trial testing the efficacy of FCV with regard to postoperative outcomes, including postoperative pulmonary complications (PPC).

The ventilation modes are conducted with CE-marked medical devices (anesthesia ventilators or medical ventilators), however these medical devices themselves are not under investigation. All CE-marked standard medical devices from varied manufacturers in use at the participating study centers will be used in full accordance with their instructions for use. FCV has shown safety and feasibility in various surgical settings, including thoracic surgery with OLV, however its feasibility in a multicenter trial has not been investigated yet.

Eligibility criteria

Qualifiers

aged ≥ 18 years; and

scheduled for elective open, video- or robot-assisted thoracic surgery with one-lung ventilation using a double-lumen tube (DLT); and

able to give written informed consent.

Disqualifiers

body weight < 40 kg;

ASA score IV - VI;

lung separation with other method than DLT (e.g. difficult airway, tracheostomy);

previous lung surgery;

Trial design

Treatments tested in this trial

  • Flow-Controlled Ventilation
  • Volume-Controlled Ventilation

Treatment groups

140 Participants
are divided into 2 treatment groups