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Clinical Trials in Turkey / NCT07602543
Active, not recruiting Observational

Lung Ultrasound Evaluation of Individualized Versus Standard PEEP on Postoperative Atelectasis in Gynecological Laparoscopy

NCT07602543 · tracked via the Priya Life Science Turkey tracker
Phase
Observational
Started
2026-02-18
Last updated
2026-05-22

Condition(s) studied

Atelectasis

Study summary

The purpose of this study is to compare two different airway pressure (PEEP) strategies during gynecological laparoscopic surgery to see which one better prevents lung collapse (atelectasis). We will compare a 'standard' fixed pressure with a 'personalized' pressure adjusted according to the patient's own lung mechanics (driving pressure). We will use lung ultrasound to check the lungs before surgery, 1 hour after surgery, and 24 hours after surgery to evaluate the results.

Eligibility

Sex
FEMALE
Min age
18 Years
Max age
65 Years
Healthy volunteers
No
Inclusion Criteria: * Female patients aged between 18 and 65 years. * American Society of Anesthesiologists (ASA) physical status I, II, or III. * Scheduled for elective laparoscopic gynecological surgery (e.g., hysterectomy, myomectomy, sacrocolpopexy). * Planned to undergo general anesthesia with endotracheal intubation. * Expected surgery duration of 2 hours or more. * Body Mass Index (BMI) ≤ 35 kg/m². Exclusion Criteria: * History of moderate-to-severe Chronic Obstructive Pulmonary Disease (COPD), clinically significant interstitial lung disease, or severe restrictive lung disease. * New York Heart Association (NYHA) class III-IV heart failure, Ejection Fraction (EF) \< 35%, or severe valvular disease. * Advanced arrhythmia or hemodynamic instability (requiring high-dose vasopressor support). * History of respiratory failure requiring mechanical ventilation within the past 4 weeks. * Clinically or radiologically confirmed lower respiratory tract infection (e.g., pneumonia) within the past 1 month. * Presence of thoracic deformity, large surgical dressings, severe subcutaneous emphysema, or any condition that hinders lung ultrasound evaluation. * Pre-existing significant atelectasis or lung consolidation (defined as a score of 3 for consolidation or ≥2 zones with a score of ≥2 on preoperative LUS). * Expected inability to perform the 24-hour postoperative ultrasound measurement (e.g., due to early discharge).

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Etlik City Hospital Ankara Turkey (Türkiye)

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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 NCT07602543 on ClinicalTrials.gov ↗ ← All trials in Turkey