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Clinical Trials in Turkey / NCT07094581
Recruiting Observational

Evaluation of the Effect of Adenoid Hypertrophy on the Masseter Muscle in Children: A Comparative Ultrasonographic Study

NCT07094581 · tracked via the Priya Life Science Turkey tracker
Sponsor
Melis AKYILDIZ
Phase
Observational
Started
2024-07-20
Last updated
2025-12-29

Condition(s) studied

Adenoid HypertrophyMasseter MuscleMalocclusion

Investigational drug(s) / intervention(s)

USG

USG: Masseter Muscle Thickness and Internal Echogenic Bands Assessed by Ultrasonography

Study summary

The goal of this observational study is to evaluate the effect of adenoid hypertrophy on the masseter muscle in children aged 3 to 8 years. The primary objectives are:

* To assess whether adenoid hypertrophy affects the thickness or structure of the masseter muscle.
* To determine whether there is a measurable difference in masseter muscle characteristics between children with and without adenoid hypertrophy.

Researchers will compare children diagnosed with adenoid hypertrophy and scheduled for adenoidectomy to healthy controls without adenoid hypertrophy.

Each participant will:

* Undergo ultrasonographic examination of the masseter muscle using a 9L linear probe (6-15 MHz), and
* Have their occlusal relationship, dental findings, age, sex, and adenoid hypertrophy grade recorded.

Eligibility

Sex
ALL
Min age
3 Years
Max age
8 Years
Healthy volunteers
Accepted
Inclusion Criteria: * Children aged between 3 and 8 years * Children diagnosed with adenoid hypertrophy * Children without any systemic disease Exclusion Criteria: * Children with a history of surgery for adenoid hypertrophy * Children who are uncooperative during clinical examination * Children with syndromes involving the maxillofacial region * Children with multiple missing teeth

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Aydın Adnan Menderes University Aydin Efeler Recruiting

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07094581 on ClinicalTrials.gov ↗ ← All trials in Turkey