Ireland
--:--IST
Starting soon Observational

Metabolic Insights: the Impact of F-18 FDG PET/CT in Adult Lymphoma

NCT06737835 · tracked via the Priya Life Science Egypt tracker
Phase
Observational
Started
2025-01-01
Last updated
2024-12-17

Condition(s) studied

Lymphoma

Investigational drug(s) / intervention(s)

18 FDG

18 FDG: 18 flurodeoxy glucose PET/CT

Study summary

1. To assess staging accuracy of F-18 FDG PET/CT in lymphoma
2. Determine the role of F-18 FDG PET/CT in monitoring treatment response and detecting relapse or residual disease in lymphoma
3. To evaluate FDG uptake correlation with histopathological subtypes and immunophenotypes as a prognostic factor.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Age: Patient must be older than 18 years. * Confirmed Diagnosis of Lymphoma: Patient must have a confirmed diagnosis of lymphoma based on histopathology and immunophenotyping. Exclusion Criteria: * Patients with Known concomitant malignancy. * Pregnancy: Pregnant women due to the potential risks associated with radiation exposure from the PET/CT scan. * Severe Renal or Hepatic Impairment: Patients with significant renal or hepatic dysfunction that could affect FDG metabolism or excretion. * Uncontrolled Diabetes: Patients with uncontrolled diabetes (blood glucose \>200 mg/dL), as it can affect FDG uptake and PET/CT results.

Primary outcome measure(s)

  • primary — 3 years
    Treatment Response Using Deauville Score for FDG Uptake Evaluation: Evaluate FDG uptake using the 5-point scale: 1. No uptake above background 2. Uptake ≤ mediastinum 3. Uptake \> mediastinum but ≤ liver 4. Moderately increased compared to liver 5. Markedly increased compared to liver X: New uptake, unlikely related to lymphoma

Trial sites (1)

FacilityCityRegionStatus
Nuclear medicine- Assiut University Hospital Asyut Egypt
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06737835 on ClinicalTrials.gov ↗ ← All trials in Egypt