- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05228977
Prevalence of Cervical Extension of the Thymus in Children (CET)
Prevalence of Cervical Extension of the Thymus in Children- A Prospective Study
Study Overview
Status
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 Type
Enrollment (Actual)
Contacts and Locations
Study Locations
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Kabul, Afghanistan, 35030
- KUMs
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None Selected
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Kabul, None Selected, Afghanistan, 35030
- Habib Ahmad Esmat
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
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 Plan
How is the study designed?
Design Details
- Observational Models: Other
- Time Perspectives: Cross-Sectional
What is the study measuring?
Primary Outcome Measures
Measure Description |
Time Frame |
|---|---|
|
As our trial has no intervention, so there were no positive or negative primary effects
|
3 months
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Collaborators and Investigators
Investigators
- Study Director: Mohammad wali Nasary, MD, KMUs
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
Other Study ID Numbers
- 0002
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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