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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00188435
Other study ID # 03-0731
Secondary ID
Status Completed
Phase Phase 1
First received September 12, 2005
Last updated April 23, 2007
Start date November 2003
Est. completion date December 2004

Study information

Verified date September 2005
Source University Health Network, Toronto
Contact n/a
Is FDA regulated No
Health authority Canada: Health Canada
Study type Interventional

Clinical Trial Summary

A comparison of chest x-ray (CXR) and Minimum dose CT (MnDCT) in the acutely ill patient. The hypothesis is that MnDCT is more sensitive than CXR in the detection of acute findings in the acutely ill patient.


Description:

A comparison of chest x-ray (CXR) and Minimum dose CT (MnDCT) in a cohort of 100 patients admitted for acute respiratory distress. Chest radiography (CXR) is compared to Minimum Dose CT (MnDCT) for the detection of consolidation;lung nodules, heart failure.


Recruitment information / eligibility

Status Completed
Enrollment 100
Est. completion date December 2004
Est. primary completion date
Accepts healthy volunteers No
Gender Both
Age group 16 Years and older
Eligibility Inclusion Criteria:

- All patients admitted for investigation of acute pulmonary embolus

Exclusion Criteria:

Study Design

Allocation: Non-Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Diagnostic


Related Conditions & MeSH terms


Intervention

Procedure:
Minimum Dose CT


Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
University Health Network, Toronto

Outcome

Type Measure Description Time frame Safety issue
Primary A comparison of CXr and MnDCT in the detection of acute findings within the thorax
See also
  Status Clinical Trial Phase
Completed NCT01949402 - A New Way of Looking at Your Lungs N/A