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