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Protective Ventilation clinical trials

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NCT ID: NCT05962125 Completed - Clinical trials for Postoperative Pulmonary Complications

The Role of Periodic Alveolar Recruitment Maneuvers in Intraoperative Protective Ventilation

REMAIN-2
Start date: August 21, 2023
Phase: N/A
Study type: Interventional

The goal of this clinical trial is to compare three open-lung strategies on respiratory function and lung injury in protective ventilation for laparoscopic anterior resection. It aims to answer whether a periodic alveolar recruitment maneuvers (PARM) strategy alone was an appropriate open-lung strategy in intraoperative protective ventilation. Patients were randomly assigned (1:1:1) to receive one of three open-lung strategies in protective ventilation: PARM alone (alveolar recruitment maneuvers [ARM] repeated every 30 min), positive end-expiratory pressure (PEEP) alone (a PEEP of 6 to 8 cm H2O), or a combination of PEEP and PARM (a PEEP of 6 to 8 cm H2O combined with ARM repeated every 30 min). The primary outcome is the mechanical power before the end of intraoperative mechanical ventilation. Secondary outcomes included the accumulative intraoperative mechanical power, an arterial partial pressure of oxygen (PaO2) / inhaled oxygen concentration (FiO2) ratio (P/F ratio) before the end of intraoperative mechanical ventilation, the rates of respiratory failure at post-anesthesia care unit (PACU) and three postoperative days, the concentration of soluble advanced glycation end products receptor (sRAGE) and Clara cell protein 16 (CC16) at the end of surgery, postoperative pulmonary complications score, postoperative hospitalization days and so on.

NCT ID: NCT03877354 Recruiting - Clinical trials for Protective Ventilation

Comparison of Tidal Volume Between Pediatric Anaesthesia and Paediatric Intensive Care Patients

TIVAC
Start date: April 1, 2019
Phase:
Study type: Observational

Paediatric anaesthesiology and paediatric intensive care unit data will be retrospectively screened for the data regarding mechanical ventilation. The primary aim will be the tidal volume setting and the secondary the level of positive end-expiration pressure (PEEP) according to the inspired oxygen fraction (FIO2), and the level of driving pressure.

NCT ID: NCT03351920 Completed - Clinical trials for Acute Respiratory Distress Syndrome

Ventilation's Parameters Applied in Emergency Medicine. A Prospective Observational Study

PARAVENT
Start date: November 7, 2017
Phase:
Study type: Observational

To prospectively assess the mechanical ventilation management when its provided by Emergency Physicians in French Hospital, and to assess complications and outcome of these patients. The study could be measure the proportion of patients developing an Acute Respiratory Failure Distress after a take care of by French Emergency Departments.