Actively Recruiting

Phase Not Applicable
Age: 19Years +
All Genders
NCT07295171

HELP Study - Towards High Throughput and Efficient Long-axial PET With Oral [18F]FDG

Led by British Columbia Cancer Agency · Updated on 2026-03-31

27

Participants Needed

1

Research Sites

52 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Typically, PET scans involve an IV injection of 18F-FDG that helps identify cancer. Patients are scanned 60 minutes after injecting 18F-FDG. This study aims to assess the feasibility of a different method of administration - oral ingestion (rather than IV) of 18F-FDG through delayed imaging to identify the optimal time for scanning after consuming the drug. The study will aim to recruit 15-24 individuals who will receive two PET scans - one using delayed oral 18F-FDG imaging and a second regular 18F-FDG. The analysis will focus on establishing a suitable protocol for this administration route while considering patient preference and image quality.

CONDITIONS

Official Title

HELP Study - Towards High Throughput and Efficient Long-axial PET With Oral [18F]FDG

Who Can Participate

Age: 19Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age 19 years or older
  • Participants who have received a standard of care [18F]FDG PET/CT and are willing to undergo a study specific oral [18F]FDG PET/CT within 2 weeks
Not Eligible

You will not qualify if you...

  • Pregnant or breastfeeding
  • Medically unstable (e.g., acute illness, unstable vital signs)
  • Urinary incontinence or use of catheter
  • Immobile, frail or vulnerable patients who cannot leave the department and would require an uptake room
  • Patients with fasting blood sugar greater than 11.0 mmol/l at the SOC PET
  • Unable to swallow
  • Patients with nasogastric tubes, percutaneous gastrostomy, or other non-anatomical nutrition routes
  • Unable to lie flat for 1 hour (first 5 participants only)
  • Claustrophobia requiring medication
  • Undergoing active treatment or assessment of upper digestive tract tumors (stomach/esophagus)
  • Unable to provide written consent
  • Patients receiving biguanide anti-hyperglycemic agents (e.g. Metformin)
  • Insulin dependent diabetics

AI-Screening

AI-Powered Screening

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Trial Site Locations

Total: 1 location

1

BC Cancer Vancouver

Vancouver, British Columbia, Canada, V5Z 4E6

Actively Recruiting

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Research Team

P

Pavithraa Administrative Research Manager

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SEQUENTIAL

Primary Purpose

OTHER

Number of Arms

1

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HELP Study - Towards High Throughput and Efficient Long-axial PET With Oral [18F]FDG | DecenTrialz