N/A
N=80
Effect of Recruitment Maneuver on Postoperative Atelectasis Assessed by Lung Ultrasound in Laparoscopic Cholecystectomy
Pulmonary Atelectasis
Bottom Line
View on ClinicalTrials.gov: NCT07324122 ↗Enrolled (actual)
80
Serious AEs
0.0%
Results posted
Feb 2026
Primary outcome: Primary: Change in Lung Ultrasound Score (LUS) — 5.2; 5.4; 8.7; 12.5 points — p=<0.001
Study Design & Population
- Study type
- Observational
- Phase
- N/A
- Interventions
- —
- Age
- Adult, Older Adult · 18+ yrs
- Sex
- All
- Sponsor
- Fatih Sultan Mehmet Training and Research Hospital
- Primary completion
- Oct 2025
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Change in Lung Ultrasound Score (LUS) |
5.2; 5.4; 8.7; 12.5; 6.3; 9.8 | <0.001 sig |
Summary
This study is an observational clinical investigation designed to evaluate perioperative lung aeration in adult patients undergoing elective laparoscopic cholecystectomy under general anesthesia. The primary objective is to assess lung status using lung ultrasound in patients aged 18 to 65 years.
A total of 80 volunteer participants will be enrolled. Lung aeration will be evaluated using lung ultrasound scoring before and after surgery. Patient demographic characteristics, medical history, intraoperative airway pressure values, and perioperative lung ultrasound scores will be recorded for analysis.
This study is conducted solely for research purposes and does not involve any drug intervention. All patients will receive standard perioperative care as determined by their attending anesthesiologist and surgical team, with no deviation from routine clinical practice. Participation is voluntary, and patients may withdraw from the study at any time without affecting their medical care.
Eligibility Criteria
Inclusion Criteria
- Adult patients scheduled for elective laparoscopic cholecystectomy under general anesthesia
- Age between 18 and 65 years
- Body mass index (BMI) < 30 kg/m²
- American Society of Anesthesiologists (ASA) physical status classification I-III
- Provision of written informed consent
Exclusion Criteria
- Refusal to participate in the study
- Emergency surgical procedures
- Body mass index (BMI) ≥ 30 kg/m²
- American Society of Anesthesiologists (ASA) physical status classification IV
Data sourced from ClinicalTrials.gov (NCT07324122). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.