Study of Breathing Pressure During Robot-Assisted Radical Prostatectomy
and Its Effect on Lung Condition After Surgery
Led by Ankara Etlik City Hospital · Updated on 2026-06-11
76
Participants Needed
1
Research Sites
3 weeks
Total Duration
AI-Summary
What this Trial Is About
This research aims to explore the connection between intraoperative driving pressure and lung ultrasound scores after surgery in men undergoing robot-assisted laparoscopic radical prostatectomy. The study focuses on how factors like pneumoperitoneum and patient positioning during this surgery may affect breathing mechanics. Researchers seek to understand how mechanical ventilation settings might influence lung conditions after the operation.
Participants will have their mechanical ventilation monitored during surgery, with special attention to driving pressure. Lung condition will be assessed objectively using lung ultrasound scores measured before anesthesia induction, 30 minutes after surgery, and 24 hours postoperatively. The study also examines anesthesia duration, mechanical power during surgery, arterial blood gas parameters, and the occurrence of postoperative pulmonary complications.
During the study, participants will undergo lung ultrasound assessments at specified times around their surgery. Researchers will collect data on ventilation parameters and blood gases at various points during anesthesia and surgery. The main outcome measured is the change in lung ultrasound score from before surgery to 24 hours after. The study will observe participants up to 24 hours postoperatively to monitor lung health and complications, with total participation spanning the surgical and immediate recovery period.
CONDITIONS
Brief Title
Intraoperative Driving Pressure and Postoperative Lung Ultrasound Score in Robot-Assisted Radical Prostatectomy
Research Team
F
Fehmi Güralp Güray, MD
S
Savas Altınsoy, MD, Prof.
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Scheduled for elective robot-assisted laparoscopic radical prostatectomy
American Society of Anesthesiologists (ASA) physical status I, II, or III
Willingness to provide written informed consent
You will not qualify if you...
Patient refusal to participate
Severe obstructive or restrictive pulmonary disease such as severe COPD or uncontrolled asthma
Body Mass Index (BMI) greater than 35 kg/m²
Pre-existing severe lung pathology or active pulmonary infection
Hemodynamic instability or severe cardiovascular disease including severe heart failure or recent myocardial infarction
Requirement for postoperative mechanical ventilation
Emergency surgery
Your Study Journey
Screening
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Observation Around Surgery
Duration - Surgery day and 24 hours postoperatively
Participants undergo lung ultrasound scans before anesthesia, 30 minutes after surgery, and 24 hours postoperatively. Mechanical ventilation and arterial blood gas parameters are monitored during surgery to study lung function changes.
3 visits (scans and assessments)
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
0
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