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About
Patients ASA I-III, undergoing laparoscopic abdominal surgery will be randomly assigned, into one of two groups, namely group C-PEEP , that will be the control group ; and group I-PEEP, where alveolar recruitment maneuvres will take place in order to identify each patient's individualized optimal PEEP. All patients will receive a standardized anesthesia regimen. The lung ultrasound score will be evaluated in all patients in the PACU and then respiratory complications will be recorded on the 24th hour, 48th hour, 7th day and 30the day, postoperatively.
Enrollment
Sex
Ages
Volunteers
Inclusion criteria
ASA I-III Laparoscopic abdominal surgery
Exclusion criteria
Severe kidney dysfunction Severe hepatic dysfunction Severe respiratory disease Severe cardiac disease Severe neuromuscular disease BMI>30 Severe intraoperative hemorrage Severe intraoperative hemodynamic instability
Primary purpose
Allocation
Interventional model
Masking
69 participants in 2 patient groups
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Central trial contact
Ioanna Pikasi
Data sourced from clinicaltrials.gov
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