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Acute DyspnoeaPhase 1NCT00188435

Comparison of CXR and MnDCT

A Phase 1 study testing Minimum Dose CT in people with Acute Dyspnoea, run by University Health Network, Toronto.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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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. Read more about this study

Who is it for?
Ages 16 years and older
Conditions the study is for
Acute Dyspnoea
What is being tested?
Minimum Dose CT
Type of treatment
Surgery or procedure
How many people
100 participants
Where
No sites listed yet
Study dates
Nov 2003to Dec 2004
Phase
Phase 1
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 16 years and older
  • All sexes
  • No healthy volunteers
  • Child, Adult, Older adult

Who may be able to join

  • All patients admitted for investigation of acute pulmonary embolus

Who cannot join

  • none

About this study

Official title: A Comparison of Chest Radiography and Minimum Dose Chest CT

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.

Read the detailed 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.

Conditions
Acute Dyspnoea
Being tested
Minimum Dose CT

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Minimum Dose CTProcedure or surgery

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. A comparison of CXr and MnDCT in the detection of acute findings within the thorax

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted16 Sep 2005 (estimated)
  2. Study startNov 2003
  3. Study completionDec 2004

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase 1
Primary purpose
Diagnosis
Allocation
Non-randomised
Intervention model
Single group
Masking
None (open label)
Enrolment
100 participants
IDs, dates and publications
ClinicalTrials.gov ID
NCT00188435
Sponsor's protocol ID
03-0731
Status last verified
Sep 2005
First submitted
12 Sep 2005
Last updated
24 Apr 2007
Results posted
No

Questions about this trial

What is this clinical trial studying?

A Phase 1 study testing Minimum Dose CT in people with Acute Dyspnoea, run by University Health Network, Toronto.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 1 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 24 Apr 2007. Status can change between updates, so confirm with the study contact before making plans.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

What does this phase mean?

Phase 1 studies test a treatment in a small group of people for the first time or in a new way, mainly to check safety and find the right dose.

Not every study follows the same path, and some studies (observational studies, device studies) have no phase.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

A comparison of CXr and MnDCT in the detection of acute findings within the thorax. It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 24 Apr 2007.

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