Actively Recruiting
Automated Intraoperative Lung Recruitment Maneuvers in Major Laparoscopic Surgery
Led by Bakirkoy Dr. Sadi Konuk Research and Training Hospital · Updated on 2026-01-21
56
Participants Needed
1
Research Sites
50 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Laparoscopic colorectal surgery is associated with an increased risk of intraoperative atelectasis due to pneumoperitoneum, Trendelenburg positioning, and prolonged anesthesia duration. Atelectasis developing during surgery may persist into the postoperative period and contribute to postoperative pulmonary complications. Automated lung recruitment maneuvers delivered by modern anesthesia ventilators may offer a standardized method to improve lung aeration and reduce atelectasis. This prospective, randomized, single-center controlled trial aims to evaluate the effect of automated intraoperative lung recruitment maneuvers on atelectasis detected by lung ultrasonography in patients undergoing elective major laparoscopic colorectal cancer surgery. Adult patients will be randomized to receive either automated lung recruitment maneuvers or standard mechanical ventilation without recruitment. Lung ultrasonography will be used to assess atelectasis at predefined perioperative time points. The primary outcome is the incidence of atelectasis detected by lung ultrasound, and secondary outcomes include postoperative pulmonary complications, length of intensive care unit stay, length of hospital stay, and perioperative hemodynamic instability.
CONDITIONS
Official Title
Automated Intraoperative Lung Recruitment Maneuvers in Major Laparoscopic Surgery
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age between 18 and 80 years
- Scheduled for elective laparoscopic colorectal cancer surgery
- American Society of Anesthesiologists (ASA) physical status I-III
You will not qualify if you...
- ASA physical status IV or higher
- Pregnancy
- Body mass index (BMI) > 40 kg/m8
- Severe chronic obstructive pulmonary disease (COPD), GOLD stage III-IV
- Advanced heart failure with left ventricular ejection fraction <35%
- Previous thoracic surgery
- Preoperative requirement for supplemental oxygen therapy
- Refusal or inability to provide informed consent
- Intraoperative conversion to open surgery
- Development of significant hemodynamic instability during lung recruitment maneuvers
AI-Screening
AI-Powered Screening
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Trial Site Locations
Total: 1 location
1
SBÜ Bakırköy Dr. Sadi Konuk Eğitim ve Araştırma Hastanesi
Istanbul, Bakırkoy, Turkey (Türkiye), 34147
Actively Recruiting
Research Team
S
Sena Gökçe Karataş
CONTACT
E
Evrim Kucur Tülübaş
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
PREVENTION
Number of Arms
2
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