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OpenTrials
Completed

NCT Number: NCT00188461

Dose Reduction in Thoracic CT

Hypothesis: Does a 50% reduction in radiation in dose significantly affect the diagnostic quality of chest CT

Completed

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Key information

Age range

16 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 1

Primary location

Toronto General Hospital

Toronto, Ontario, Canada

About this study

Patients with Lymphoma are recruited and have a follow up CT performed at 50% of the standard exposure parameters. The studies are compared for image quality with a recent (<3 months) thoracic CT performed at standard exposure parameters.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Patients with Lymphoma

Exclusion criteria

  • No recent (<3 months) thoracic CT

Treatment and study plan

CT Thorax

Device

Primary outcomes

  1. Evaluating the diagnostic quality of thoracic CT exams performed at 50% of standard dose parameters

Sponsors and collaborators

Lead sponsor

University Health Network, Toronto

Other

Registry information

Official study title

Dose Reduction in Thoracic CT: A Comparison of on Line Automatic Dose Reduction and a 50% Reduction in Dose

Important dates

Study start
2004
Study completion
2005
First posted
Sep 16, 2005
Registry last updated
Apr 23, 2007

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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