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Clinical trial

Evaluation of 18F-2-fluoro-2-deoxy-D-glucose Produced by a New Manufacturer, for Safety, Through the Identification of Adverse Events, and Efficacy, Through the Evaluation of Its Ability, When Utilized in Performance of a Positron Emission Tomography Computed Tomography Scan, to Correctly Distinguish Benign From Malignant Solitary Pulmonary Nodules.

NCT04615156 is registered in ClinicalTrials.gov with Eastern Health, Canada as lead sponsor.

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Registry record

As filed in ClinicalTrials.gov.

Title
Evaluation of 18F-2-fluoro-2-deoxy-D-glucose Produced by a New Manufacturer, for Safety, Through the Identification of Adverse Events, and Efficacy, Through the Evaluation of Its Ability, When Utilized in Performance of a Positron Emission Tomography Computed Tomography Scan, to Correctly Distinguish Benign From Malignant Solitary Pulmonary Nodules.
Lead sponsor
Eastern Health, Canada
Phase
Phase 3
Overall status
Not yet recruiting
Start date
November 1, 2020
Completion date
November 1, 2027
Enrollment
10,000 (estimated)
Sites
Not reported

Conditions

As the registry lists them; a condition with its own page is linked.

18f-2-fluoro-2-deoxy-d-glucose, adverse event, oncology, solitary pulmonary nodule