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RECRUITING
NCT04706910
PHASE3

18F-DOPA II - PET Imaging Optimization

Sponsor: University of Alberta

View on ClinicalTrials.gov

Summary

A single centre non-randomized, non-blinded phase III prospective cohort study of 18F-DOPA PET/CT imaging in specific patient populations: 1. Pediatric patients (less than 18 years old) with congenital hyperinsulinism. 2. Pediatric patients (less than 18 years old) with neuroblastoma. 3. Pediatric (less than 18 years old) or Adult patients (18 or older) with known or clinically suspected neuroendocrine tumor. 4. Adult patients (18 or older) with a clinical suspicion of Parkinson's disease or Lewy body dementia. 5. Pediatric (less than 18 years old) or Adult patients (18 or older) with brain tumors. Image optimization (the primary study objective) and gallbladder activity pattern (the secondary objective) will be evaluated.

Key Details

Gender

All

Age Range

Any - Any

Study Type

INTERVENTIONAL

Enrollment

800

Start Date

2021-01-20

Completion Date

2027-12

Last Updated

2026-02-09

Healthy Volunteers

No

Interventions

DRUG

18F-DOPA

All participants will receive an intravenous injection of 18F-DOPA (4MBq/kg; minimum 110 MBq, maximum 600 MBq) for this study

DRUG

Furosemide Injection

Some participants will receive an intravenous injection of furosemide (40mg, single dose)

Locations (1)

WC Mackenzie Health Science Centre / University of Alberta Hospital

Edmonton, Alberta, Canada