NCT02689908

Brief Summary

The adjustment of radiation dose in many CT protocol are based on body mass index(BMI) or weight of the patient. In the literature, neck circumference (NC) has been reported as a new anthropometric parameter indicating the body mass for the upper body. NC may be an important landmark in the determination of the low dose protocols for upper body CT examinations such as neck, chest and coronary CT.

Trial Health

43
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
100

participants targeted

Target at P50-P75 for not_applicable

Timeline
Completed

Started May 2015

Shorter than P25 for not_applicable

Geographic Reach
1 country

2 active sites

Status
unknown

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

May 1, 2015

Completed
9 months until next milestone

First Submitted

Initial submission to the registry

January 31, 2016

Completed
1 day until next milestone

Primary Completion

Last participant's last visit for primary outcome

February 1, 2016

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

February 1, 2016

Completed
23 days until next milestone

First Posted

Study publicly available on registry

February 24, 2016

Completed
Last Updated

February 24, 2016

Status Verified

February 1, 2016

Enrollment Period

9 months

First QC Date

January 31, 2016

Last Update Submit

February 18, 2016

Conditions

Keywords

Thorax CTLow DoseBody Mass IndexNeck Circumference

Outcome Measures

Primary Outcomes (1)

  • The measurement of neck circumference of the patients undergoing non-enhanced thorax CT

    Before CT examination, during patient preparation, neck circumference was measured horizontally at the level of the cyricoid cartilage by a non-elastic flexible tape (centimeter, cm)

    1 year

Secondary Outcomes (3)

  • The measurement of weight of the patients undergoing non-enhanced thorax CT

    1 year

  • The measurement of height of the patients undergoing non-enhanced thorax CT

    1 year

  • Calculating the body mass index (BMI) using the results of each patient measured in outcome 2 and outcome 3.

    1 year

Study Arms (1)

The patients underwent thorax CT

OTHER

The patients refered to radiology service underwent thorax computed tomography without contrast material for the evaluation of various complaints such as dyspnea, hemoptysis and pulmonary infections.

Radiation: computed tomography

Interventions

low dose protocol of thorax ct

The patients underwent thorax CT

Eligibility Criteria

Age18 Years - 80 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • clinical diagnosis of pulmonary diseases
  • participants who can be referred to radiology for diagnostic imaging
  • participants who allowed to be taken somatometric measurements

You may not qualify if:

  • participants who did not allow to be taken somatometric measurements
  • participants with incomplete data (such as missing weight or height data)
  • pediatric and pregnant patients

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (2)

Ferhat

Van, Van, 65002, Turkey (Türkiye)

COMPLETED

Erdem

Van, Van, Turkey (Türkiye)

RECRUITING

Related Publications (1)

  • Ghoshhajra BB, Engel LC, Major GP, Verdini D, Sidhu M, Karolyi M, Abbara S, Hoffmann U, Kalra M, Brady TJ. Direct chest area measurement: A potential anthropometric replacement for BMI to inform cardiac CT dose parameters? J Cardiovasc Comput Tomogr. 2011 Jul-Aug;5(4):240-6. doi: 10.1016/j.jcct.2011.06.003. Epub 2011 Jun 12.

Related Links

Study Officials

  • serkan arıbal

    Aksaz Military Hospital

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NA
Masking
NONE
Purpose
DIAGNOSTIC
Intervention Model
SINGLE GROUP
Sponsor Type
OTHER GOV
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
staff radiology specialist, department of radiology

Study Record Dates

First Submitted

January 31, 2016

First Posted

February 24, 2016

Study Start

May 1, 2015

Primary Completion

February 1, 2016

Study Completion

February 1, 2016

Last Updated

February 24, 2016

Record last verified: 2016-02

Data Sharing

IPD Sharing
Will share

Locations