Actively Recruiting
Diaphragm Ultrasound İn Children With OSAS
Led by Istanbul University · Updated on 2026-02-02
60
Participants Needed
1
Research Sites
51 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
This is a prospective observational study evaluating perioperative diaphragmatic function by ultrasonography in children aged 1-12 years undergoing elective surgery under general anesthesia. Participants will be classified preoperatively based on the parent-completed Pediatric Sleep Questionnaire (PSQ). Children with suspected obstructive sleep apnea syndrome who are scheduled for adenotonsillectomy will form the study group, while children without clinical findings suggestive of obstructive sleep apnea who are scheduled for elective non-airway-related otolaryngologic surgeries will serve as controls. Diaphragm ultrasound assessments will be performed before and after surgery in the supine position during spontaneous breathing. Measurements will include diaphragmatic thickness at end-inspiration and end-expiration, diaphragmatic thickening fraction, and diaphragmatic excursion during quiet and deep breathing. The primary objective is to compare diaphragmatic excursion and thickening fraction between groups. Secondary objectives include evaluating the association between perioperative respiratory parameters, postoperative recovery, and diaphragm ultrasound measures.
CONDITIONS
Official Title
Diaphragm Ultrasound İn Children With OSAS
Who Can Participate
Eligibility Criteria
You may qualify if you...
- ASA physical status I-II
- Children aged 1 to 12 years
- Scheduled to undergo elective surgery under general anesthesia
- Written informed consent obtained from parents or legal guardians
- Availability of a completed pediatric sleep questionnaire (PSQ)
You will not qualify if you...
- Patients younger than 1 year or older than 12 years
- Presence of a neuromuscular disease
- Use of medications that may affect neuromuscular function
- Diaphragmatic paralysis
- ASA physical status III-IV
- Refusal to participate in the study or failure to provide informed consent
- Body mass index (BMI) > 35 kg/m�b2
AI-Screening
AI-Powered Screening
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Trial Site Locations
Total: 1 location
1
Istanbul University, Department of Anesthesiology
Istanbul, Fatih, Turkey (Türkiye), 34093
Actively Recruiting
Research Team
D
Demet Altun, Professor
CONTACT
F
Furkan Kelebek, Resident
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
2
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