- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05528159
Lung Ultrasound Score (LUS) Change in Robotic and Laparoscopic Urologic Surgeries
Perioperative Lung Ultrasound Score (LUS) Changes in Robotic and Laparoscopic Urologic Surgeries: A Prospective Observational Trial
Robotic and laparoscopic surgeries are tend to cause lung atelectasis due to the insufflation of CO2 into abdomen. However, ultrasonographic measurement for this phenomenon and its clinical use is not well investigated. In this particular study, It is aimed to observe lung ultrasound score (LUS) changes in robotic and laparoscopic supine position surgeries such as prostatectomies and cystectomies. LUS is a pragmatic measurement method that calculates the degree of atelectasis and consolidation in the lungs. Both hemithoraxes are separated into 3 different segments with vertical lines (one between the parasternal line and anterior axillary line, one between the anterior and posterior axillary line, and one posterior to the posterior axillary line). These vertical segments are also divided into two with an horizontal line on the nipple. Lung ultrasonography is applied in all 12 zones for both lungs in the intercostal regions and a scoring system is used. Accordingly, pure A lines (transverse frequent lines) reflects normal lung tissue with no consolidation and scored as zero points (Also named "A"). If less than 4 B lines (vertical lines reflecting some degree of consolidation) is observed, it refers to 1 point (named "B1"). 4 or more B lines refers to 2 points (B2), and if wide and coalesced B lines or patchy pleural line is observed that refers to 3 points (C). All evaluations will be made in supine position.
In this trial, LUS will be applied in three different time points:
T1: 5 minutes after orotracheal intubation T2: At the end of surgery, before extubation (under deep anesthetic state) T3: 30 minutes after extubation, in postanesthesia care unit During the surgery and the postoperative care period standart monitorization and mechanical ventilation data will be gathered. Also intraoperative and postoperative blood gas analysis will be obtained to observe oxygenation changes.
This study is planned as a prospective observational study and our hypothesis is that LUS scores would be lower in acute postoperative period with robotic and laparoscopic surgeries. Therefore primary outcome is the numeric change in T3 and T1. Secondarily, LUS scores will be evaluated between robotic group and laparoscopic group patients for all time points.
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
-
-
-
Istanbul, Turkey
- Istanbul University
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- >18 years
- Laparoscopic urologic surgeries
- Robotic urologic surgeries
- Surgeries under supine and trendelenburg position
Exclusion Criteria:
- Known lung disease
- Emergency surgeries
- Known cardiac failure
- Known pulmonary hypertension
- Patients receiving inhaled agents
- Patients requiring lateral position surgeries
Study Plan
How is the study designed?
Design Details
- Observational Models: Cohort
- Time Perspectives: Prospective
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
Robotic and Laparoscopic Urologic Surgery Group
Patients scheduled for robotic/laparoscopic urologic surgeries that will be performed under supine and trendelenburg position
|
Patients will receive intraabdominal CO2 insufflation and will be operated under trendelenburg position
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
LUS change between T3 and T1
Time Frame: Up to 6 hours
|
LUS will be evaluated at the start of the surgery right after intubation (T1) and 30 minutes after the extubation (T3).
LUS refers to "lung ultrasound score" .
Accordingly, one hemithorax is divided into 6 zones where the ultrasound probe is placed.
If there is only A lines (no consolidation) observed, it is accepted as zero points.
If there are three or less B lines (vertical lines that move with the respiration), it refers to 1 point.
Four or more vertical B lines refer to 2 points, and lastly distinct visible atelectasis with converged B lines and disrupted pleura refer to 3 points.
In total, ultrasonography is applied on 12 different zones, and sum of the points show the actual LUS.
Less points mean lungs with better condition, and higher points reflect lungs with atelectasis and consolidation.
Therefore a 36 points LUS indicates severely injured lungs.
|
Up to 6 hours
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Delta T (T2-T1) and surgical duration relation
Time Frame: Up to 6 hours
|
Intraoperative LUS change will be evaluated in relation to surgical duration.
LUS refers to "lung ultrasound score" .
Accordingly, one hemithorax is divided into 6 zones where the ultrasound probe is placed.
If there is only A lines (no consolidation) observed, it is accepted as zero points.
If there are three or less B lines (vertical lines that move with the respiration), it refers to 1 point.
Four or more vertical B lines refer to 2 points, and lastly distinct visible atelectasis with converged B lines and disrupted pleura refer to 3 points.
In total, ultrasonography is applied on 12 different zones, and sum of the points show the actual LUS.
Less points mean lungs with better condition, and higher points reflect lungs with atelectasis and consolidation.
Therefore a 36 points LUS indicates severely injured lungs.
|
Up to 6 hours
|
|
Perioperative PaO2 analysis and its relation to T3 LUS
Time Frame: Up to 6 hours
|
PaO2 values will be evaluated at T3 time point to observe its relation with LUS scores.
LUS refers to "lung ultrasound score" .
Accordingly, one hemithorax is divided into 6 zones where the ultrasound probe is placed.
If there is only A lines (no consolidation) observed, it is accepted as zero points.
If there are three or less B lines (vertical lines that move with the respiration), it refers to 1 point.
Four or more vertical B lines refer to 2 points, and lastly distinct visible atelectasis with converged B lines and disrupted pleura refer to 3 points.
In total, ultrasonography is applied on 12 different zones, and sum of the points show the actual LUS.
Less points mean lungs with better condition, and higher points reflect lungs with atelectasis and consolidation.
Therefore a 36 points LUS indicates severely injured lungs.
|
Up to 6 hours
|
|
Intergroup oxygenation difference
Time Frame: Up to 6 hours
|
T3 PaO2 values will be compared in laparoscopic and robotic surgery groups.
|
Up to 6 hours
|
|
Perioperative PaCO2 analysis and its relation to T3 LUS
Time Frame: Up to 6 hours
|
PaCO2 values will be evaluated at T3 time point to observe its relation with LUS scores.
LUS refers to "lung ultrasound score" .
Accordingly, one hemithorax is divided into 6 zones where the ultrasound probe is placed.
If there is only A lines (no consolidation) observed, it is accepted as zero points.
If there are three or less B lines (vertical lines that move with the respiration), it refers to 1 point.
Four or more vertical B lines refer to 2 points, and lastly distinct visible atelectasis with converged B lines and disrupted pleura refer to 3 points.
In total, ultrasonography is applied on 12 different zones, and sum of the points show the actual LUS.
Less points mean lungs with better condition, and higher points reflect lungs with atelectasis and consolidation.
Therefore a 36 points LUS indicates severely injured lungs.
|
Up to 6 hours
|
|
Intraoperative compliance change
Time Frame: Up to 6 hours
|
dynamic compliance change between T2 and T1.
|
Up to 6 hours
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 2022/1056
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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