18F-2-fluoro-2-deoxy-D-glucose in Positron Emission Tomography Computed Tomography

NCT04615156 | Not Yet Recruiting Phase 3

• 1 other identifier: 231364
• Study Type: interventional
• Target: 10,000
• Locations: 0 countries
• Sites: N/A

Brief Summary

The study objectives are as follows:

• To determine the safety of trial 18F-2-fluoro-2-deoxy-D-glucose, produced by a new manufacturer, by surveillance for adverse events in patients having Positron Emission Tomography Computed Tomography scans in a comprehensive program for indications including, but not limited to, oncology, neurology, cardiac and infectious/inflammatory processes.
• To determine the efficacy of 18F-2-fluoro-2-deoxy-D-glucose Positron Emission Tomography in differentiating benign from malignant solitary pulmonary nodules and calculate sensitivity, specificity, and accuracy using pathologic confirmation as the gold standard when available, or greater than 6 month follow up stability on Computed Tomography scan when not. The purpose of performing this clinical trial is to provide local access of 18F-2-fluoro-2-deoxy-D-glucose to the patients of Newfoundland and Labrador. This product has been offered to patients over the last three years by transporting from facilities outside of the province. There have been significant delays in access and in fact, times where 18F-2-fluoro-2-deoxy-D-glucose has not been available through this process. This has caused delays and limitations of treatments for patients who rely on Positron Emission Tomography Computed Tomography scans for diagnosis.

Conditions

Solitary Pulmonary Nodule; Oncology; 18F-2-fluoro-2-deoxy-D-glucose; Adverse Event

Keywords

18F-2-fluoro-2-deoxy-D-glucose; Adverse Event; Solitary Pulmonary Nodule; Oncology

Outcome Measures

Primary Outcomes (1)

• Measuring the safety of 18F-2-fluoro-2-deoxy-D-glucose produced by a new manufacturer by evaluating for any adverse events that occur during their Positron Emission Tomography Computed Tomography scan appointment.

  Evaluation for any adverse events after administration of 18F-2-fluoro-2-deoxy-D-glucose produced by Eastern Health in the Nuclear and Molecular Medicine Department who is a new manufacturer

  For the length of time required to perform informed consent, the scan, and follow-up interview for adverse events, approximately 4 hours

Secondary Outcomes (1)

• Evaluation of the sensitivity, specificity and accuracy of 18F-2-fluoro-2-deoxy-D-glucose in the assessment of solitary pulmonary nodules compared to anatomic pathology, or more than 6 month follow-up stability when not available.

  Variable, from the time of the scan to appropriate follow-up (either biopsy or follow-up imaging that occurs more than 6 months after the Positron Emission Tomography Computed Tomography study)

Study Arms (1)

Evaluation for adverse events from 18F-2-fluoro-2-deoxy-D-glucose produced by a new manufacturer

EXPERIMENTAL

Drug: 18F-2-fluoro-2-deoxy-D-glucose

Interventions

18F-2-fluoro-2-deoxy-D-glucose DRUG

Administration of 18F-2-fluoro-2-deoxy-D-glucose for the purposes of diagnosis.

Evaluation for adverse events from 18F-2-fluoro-2-deoxy-D-glucose produced by a new manufacturer

Eligibility Criteria

• Sex: all
• Healthy Volunteers: No
• Age Groups: Child (0-17), Adult (18-64), Older Adult (65+)

You may qualify if:

• Known or suspected disease for which 18F-2-fluoro-2-deoxy-D-glucose Positron Emission Tomography Computed Tomography is appropriate for the investigation of. This includes, but is not limited to: Known or suspected cancer, neurological disorders (dementia or epilepsy), cardiac conditions (inflammation or myocardial viability), known or suspected presence of infection/inflammation process
• Patients must satisfy all the following:
• Able to provide written informed consent, or consent obtained from appropriate guardian
• Able to tolerate the physical and logistic requirements of completing a Positron Emission Tomography Computed Tomography scan

You may not qualify if:

• Pregnant women: if there is any possibility of pregnancy, a blood Beta Human Chorionic Gonadotropin level will be obtained as per Eastern Health policy.
• Patients unwilling or unable to stop breast feeding for 12 hours
• Patients who are too medically unstable to tolerate the uptake period or lie flat for the duration of the scan
• Patients who exceed the safe weight limit of the Positron Emission Tomography Computed Tomography scanner bed (500 lbs.) or who cannot fit through the bore (70 cm diameter)
• Patients unwilling to proceed with scan (I.e. claustrophobia) prior to injection
• If patients inability to follow staff direction causes a safety hazard prior to injection

Sponsors & Collaborators

• Eastern Health, Canada: lead

MeSH Terms

Conditions

Solitary Pulmonary Nodule; Neoplasms

Condition Hierarchy (Ancestors)

Lung Diseases; Respiratory Tract Diseases

Central Study Contacts

Andrea Morgan, MNRN

CONTACT

709-777-1133; andrea.morgan@easternhealth.ca

Jeffery Flemming, MD

CONTACT

709-777-1133; jeffery.flemming@easternhealth.ca

Study Design

• Study Type: interventional
• Phase: phase 3
• Allocation: NA
• Masking: NONE
• Purpose: DIAGNOSTIC
• Intervention Model: SINGLE GROUP
• Sponsor Type: OTHER
• Responsible Party: PRINCIPAL INVESTIGATOR
• PI Title: Clinical Chief, Nuclear and Molecular Medicine, Eastern Health

Study Record Dates

• First Submitted: October 28, 2020
• First Posted: November 4, 2020
• Study Start: November 1, 2020
• Primary Completion (Estimated): November 1, 2027
• Study Completion (Estimated): November 1, 2027
• Last Updated: November 4, 2020

Record last verified: 2020-11

Data Sharing

• IPD Sharing: Will not share