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Computed Tomography (CT) in Head and Neck Patients

Primary Purpose

Lung Tumors

Status
Terminated
Phase
Phase 1
Locations
Canada
Study Type
Interventional
Intervention
CT thorax
Sponsored by
University Health Network, Toronto
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional diagnostic trial for Lung Tumors

Eligibility Criteria

16 Years - undefined (Child, Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Patients with squamous cell carcinoma of the head and neck Exclusion Criteria: None

Sites / Locations

  • Princess Margaret Hospital

Outcomes

Primary Outcome Measures

Detection of lung metastases

Secondary Outcome Measures

Full Information

First Posted
September 12, 2005
Last Updated
December 14, 2010
Sponsor
University Health Network, Toronto
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1. Study Identification

Unique Protocol Identification Number
NCT00188656
Brief Title
Computed Tomography (CT) in Head and Neck Patients
Official Title
Minimum Dose CT in the Detection of Lung Nodules in Patients With Head and Neck Cancer
Study Type
Interventional

2. Study Status

Record Verification Date
December 2010
Overall Recruitment Status
Terminated
Why Stopped
insufficient recruitment
Study Start Date
August 2003 (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
September 2006 (undefined)

3. Sponsor/Collaborators

Name of the Sponsor
University Health Network, Toronto

4. Oversight

5. Study Description

Brief 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.
Detailed 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

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Lung Tumors

7. Study Design

Primary Purpose
Diagnostic
Study Phase
Phase 1
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
100 (false)

8. Arms, Groups, and Interventions

Intervention Type
Procedure
Intervention Name(s)
CT thorax
Primary Outcome Measure Information:
Title
Detection of lung metastases

10. Eligibility

Sex
All
Minimum Age & Unit of Time
16 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients with squamous cell carcinoma of the head and neck Exclusion Criteria: None
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Narinder Paul, FRCP C
Organizational Affiliation
University Health Network, Toronto
Official's Role
Principal Investigator
Facility Information:
Facility Name
Princess Margaret Hospital
City
Toronto
State/Province
Ontario
Country
Canada

12. IPD Sharing Statement

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Computed Tomography (CT) in Head and Neck Patients

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