🇮🇪Ireland
16°C Partly Cloudy · Dublin
Live Updates
--:--:-- IST
Contributor sign in
Latest
Clinical Trials in Turkey / NCT06994780
Active, not recruiting Not applicable

Lung Ultrasound Evaluation of the Effects of PEEP and Recruitment Strategies Adjusted for Intraoperative Dynamic Compliance on Postoperative Respiratory Complications in Obese Patients Planned for Laparoscopic Surgery

NCT06994780 · tracked via the Priya Life Science Turkey tracker
Phase
Not applicable
Started
2025-01-01
Last updated
2025-05-29

Condition(s) studied

ObesityPostoperative Bariatric SurgeryLaparoscopic SurgeryIndividualized PEEP Treatment Strategy

Investigational drug(s) / intervention(s)

dynamic compliance guided PEEP titration

dynamic compliance guided PEEP titration: In order to find the individualized optimal PEEP value, PEEP will be increased at 2-minute intervals with a maximum peak pressure of 45 cmH2O and a driving pressure of 15 cmH2O. Recruitment will be performed. When the target is reached, the PEEP value will be adjusted to the value at which the highest dynamic compliance is achieved by decreasing it.

Study summary

This study aims to investigate the effects of the personalized application of respiratory pressures applied to patients undergoing laparoscopic bariatric surgery when they are connected to a ventilator under general anesthesia, on the postoperative period. The effects of the ventilation practices that are fixed in routine practice and revised according to various variables during the surgery during artificial respiration after intubation under general anesthesia will be examined with ultrasonography. No change will be made to the routine anesthesia practice for this purpose, the pressure values in the ventilator under general anesthesia will be adjusted during the surgery within the framework of the values used in anesthesia practice. After the surgery, the lung area will be examined with ultrasound in the recovery unit and the findings will be recorded. This study does not have any undesirable effects or risks. This study does not include any interventional procedures.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
Accepted
Inclusion Criteria: \- Patients over the age of 18, with a body mass index of 35 and above, and who are scheduled for laparoscopic bariatric surgery will be included in our study. Exclusion Criteria: * Patients with advanced COPD, * Patients with a history of pneumothorax, * Patients with lung bullae, * Patients who have undergone thoracic surgery, * Patients with a diagnosis of major cardiac disease (valve diseases, heart failure, systolic dysfunction), * Patients with severe respiratory failure, * Patients with previous pulmonary surgery will not be included in the study.

Primary outcome measure(s)

Trial sites (2)

FacilityCityRegionStatus
Marmara University Pendik Training and Reseach Hospital Istanbul Pendik
Marmara University Pendik Training and Research Hospital Istanbul pendik

More Marmara University Pendik Training and Research Hospital trials in Turkey

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06994780 on ClinicalTrials.gov ↗ ← All trials in Turkey