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Clinical Trial Details — Status: Terminated

Administrative data

NCT number NCT00188656
Other study ID # 03-0467
Secondary ID
Status Terminated
Phase Phase 1
First received September 12, 2005
Last updated December 14, 2010
Start date August 2003
Est. completion date September 2006

Study information

Verified date December 2010
Source University Health Network, Toronto
Contact n/a
Is FDA regulated No
Health authority Canada: Health Canada
Study type Interventional

Clinical Trial Summary

This study is conducting a comparison of chest x-ray (CXR) and minimum dose thoracic CT (MnDCT) in the detection of lung nodules (metastases) in patients with head and neck carcinoma.


Description:

A comparison of chest x-ray (CXR) and minimum dose thoracic CT (MnDCT)in the detection of lung nodules (metastases) in patients with head and neck carcinoma


Recruitment information / eligibility

Status Terminated
Enrollment 100
Est. completion date September 2006
Est. primary completion date
Accepts healthy volunteers No
Gender Both
Age group 16 Years and older
Eligibility Inclusion Criteria:

- Patients with squamous cell carcinoma of the head and neck

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:
CT thorax


Locations

Country Name City State
Canada Princess Margaret Hospital Toronto Ontario

Sponsors (1)

Lead Sponsor Collaborator
University Health Network, Toronto

Country where clinical trial is conducted

Canada, 

Outcome

Type Measure Description Time frame Safety issue
Primary Detection of lung metastases
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