Prevalence of Cervical Extension of the Thymus in Children

Completed

• Conditions: Prevalence of Cervical Extension of the Thymus

• Registration Number: NCT05228977
• Lead Sponsor: Kabul University of Medical Sciences

Brief Summary

This prospective, observational study included all pediatric patients who were referred to the radiology department for neck ultrasonography between August-October 2018. A high-frequency probe was implemented and 220 patients were examined.

Detailed Description

This prospective single-centered study was approved by the Institutional Review Board for Ethical Issues in Clinical Research and is compatible with the Declaration of Helsinki. The patients referred to the radiology department for the neck US with various clinical indications between August-October 2018 were included in the study. The informed consent was taken from the parents of the patients. The patients who had any systemic illness, were treated for malignancy or had any history of lower neck or chest surgery, were excluded.

The neck US was performed by two radiologists. The length of the extended thymus, from the upper margin of the manubrium to the superior edge of the thymic tissue on the transverse plane, was measured in millimeters and recorded.

al analysis of the data was performed in SPSS, Version 24 program (IBM, Armonk, New York). Pearson Chi-Square Test was used in comparing categorical data between groups.

Study Timeline

• Study Start: 2018-08-01
• Primary Completion: 2018-10-01
• Study Completion: 2018-10-30
• Study First Submitted: 2022-01-26
• Status Verified: 2022-02
• Study First Submitted QC: 2022-02-06
• Last Update Submitted: 2022-02-06
• Study First Posted: 2022-02-08
• Last Update Posted: 2022-02-08

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 220

Inclusion Criteria

• The patients referred to the radiology department for the neck US with various clinical indications between August-October 2018 were included in the study.

Exclusion Criteria

• The patients who had any systemic illness, were treated for malignancy, or had any history of lower neck or chest surgery, were excluded.

Study & Design

• Study Type: OBSERVATIONAL
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
0	3 months	As our trial has no intervention, so there were no positive or negative primary effects

Trial Locations

Locations (2)

Habib Ahmad Esmat; 🇦🇫 Kabul, None Selected, Afghanistan

KUMs; 🇦🇫 Kabul, Afghanistan