Actively Recruiting

Age: 1Year - 12Years
All Genders
Healthy Volunteers
NCT07380321

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

Age: 1Year - 12Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

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)
Not Eligible

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

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Istanbul University, Department of Anesthesiology

Istanbul, Fatih, Turkey (Türkiye), 34093

Actively Recruiting

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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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