- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06072885
Evaluation of Perioperative Lung Ultrasound Scores in Laparoscopic Pediatric Surgeries
Prospective Observational Evaluation of Perioperative Lung Ultrasound Scores in Laparoscopic Pediatric Surgeries
Laparoscopic surgeries require carbon-dioxide into the abdomen which may occasionally lead to atelectasis. The extent of this atelectasis is not well documented in peri-operative period although it has been extensively researched in critical care set up. In this study, it is aimed to observe the ultrasonographic condition of lungs in laparoscopic pediatric surgeries. The hypothesis was the Lung Ultrasound Scores would worsen in those surgeries by the end of the operation. Aged between 1-18 years pediatric patients who are scheduled for laparoscopic surgeries will be included in the study to observe the changes in the lung visuals throughout the operation. For that, after safe endotracheal intubation first ultrasonography will be performed for the first (T1) time, and the second ultrasonography will be performed once the surgery is finished and before extubation (T2). Lastly, the third evaluation will be performed after 30 minutes in post anesthesia care unit (T3). Lung Ultrasound Score (LUS) is calculated as follows: Both hemi-thoraxes are divided into 6 different zones, and depending on the number of B-lines, which happens due to aeration loss in lung tissue, every zone is scored. If there is no B-line, it is zero points. If the B-lines in the visual lower than 4, the area is scored as 1 point. The areas with B-lines more than 3 is scored as 2 points. Furthermore, if there is any disruption on the pleural face, then the area is scored as 3 points. Accordingly, the worst case scenario refers 36 points, meaning the less the points the better the lung aeration.
Primary outcome is defined as T2 LUS which will show the actual condition of at the end of the surgery. For that, T1 scores and T2 scores will be compared. The secondary outcomes include T3 LUS, (T3-T1)LUS, intraoperative hemodynamics, length of stay in Post Anesthesia Care Unite, postoperative aldrete scores for discharging to ward, and intraoperative ventilation variables.
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
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-
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Istanbul, Turkey
- Istanbul University Istanbul Faculty of Medicine
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- Laparoscopic pediatric surgeries
- Aged between 1-18 years
Exclusion Criteria:
- Patients with Constitutional lung diseases
- Patients with Heart failure
- Patients with pulmonary hypertension
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
Laparoscopic pediatric surgery
Pediatric patients who are scheduled for laparoscopic surgeries in supine position (e.g.
laparoscopic appendectomy, laparoscopic cholecystectomy, laparoscopic nissen fundoplication)
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Pediatric Laparoscopic Surgery patients will be undergone Lung Ultrasound Scoring (LUS) at multiple times perioperatively.
LUS is a pragmatic calculation reflecting lung aeration.
Thorax is divided into 12 areas, and in every one of them LUS is applied to observe the lung condition.
For that, if there are B-lines less than 4 in one area, it is scored as 1 point.
For the areas containing more than 3 B-lines, it is scored as 2 points, and if there is any distortion on the pleural line, it is scored as 3 points.
The areas with no B-lines is scored as 0 points.
Considering these details, lungs with best conditions will reflect 0 points whereas the worst condition lungs will reflect 36 points.
LUS will be performed after intubation, before extubation, and after 30th minute in the post anesthesia care unit
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Lung Ultrasound Score in T2 time point (After surgery finish, before extubation)
Time Frame: Up to 4 hours
|
LUS is a pragmatic calculation reflecting lung aeration.
Thorax is divided into 12 areas, and in every one of them LUS is applied to observe the lung condition.
For that, if there are B-lines less than 4 in one area, it is scored as 1 point.
For the areas containing more than 3 B-lines, it is scored as 2 points, and if there is any distortion on the pleural line, it is scored as 3 points.
The areas with no B-lines is scored as 0 points.
Considering these details, lungs with best conditions will reflect 0 points whereas the worst condition lungs will reflect 36 points.
T2 LUS will be compared to T1 LUS to observe possible significant change in lung condition.
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Up to 4 hours
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Lung Ultrasound Score in T3 time point (30 minutes after admission to post anesthesia care unit
Time Frame: Up to 4 hours
|
To measure Thorax is divided into 12 areas, and in every one of them LUS is applied to observe the lung condition.
For that, if there are B-lines less than 4 in one area, it is scored as 1 point.
For the areas containing more than 3 B-lines, it is scored as 2 points, and if there is any distortion on the pleural line, it is scored as 3 points.
The areas with no B-lines is scored as 0 points.
Considering these details, lungs with best conditions will reflect 0 points whereas the worst condition lungs will reflect 36 points.
T3 LUS will be compared to T1 LUS to observe possible significant change in lung condition.
|
Up to 4 hours
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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
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 2023/796
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
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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