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NCT Number: NCT07306975

Comparative Analysis of SUV Measurements Using Different Correction Methods in Oncological PET/CT Imaging.

-To measure SUVs by using different correction methods in oncological PET/CT imaging.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

About this study

-To compare between SUV measurements in the tumor and liver using different standardizing parameters such as: body weight, lean body mass and body surface area.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Cancer patients (> 18 years old) referred to nuclear medicine unit to do F18-FDG PET/CT study.

Exclusion criteria

  • Patients < 18 years old.
  • Patients with increased FDG uptake on tissue associated with non-malignant causes such as diffuse bone marrow FDG uptake or inflammatory.
  • Patients with extensive metastasis.

Treatment and study plan

PET/CT with 18-FDG

Device
  • Patients will fast for at least 4 hrs before imaging with blood glucose level (<200 mg/dl) before intravenous administration of F18-FDG.
  • Imaging will be performed approximately 45 to 60 min after 18F-FDG injection, an imaging field of view from the base of skull to mid-thighs with the arms above the head whenever possible is used or otherwise the arms are positioned beside the body.

Primary outcomes

  1. -To measure SUVs by using different correction methods in oncological PET/CT imaging.

    Time frame: 1/12/2025 to 1/10/2027

    -To compare between SUV measurements in the tumor and liver using different standardizing parameters such as: body weight, lean body mass and body surface area.

Secondary outcomes

  1. To determine if SUVbsa is more accurate than SUVbw in obese patients.

    Time frame: 1/12/2025 to 1/10/2027

    -To determine if ''normalization of FDG uptake for the body surface area'' (SUVbsa) is independent of the patient's body size and is more reliable than SUVbw.

Study contacts

Contact information is provided by the study sponsor or research team.

Aya Kamel Hamed Ahmed, Resident doctor

CONTACT

[email protected]

+2001097763423

HebatAllah Ahmed AbdelRaoof Askar, Assistant Professor, doctor

CONTACT

[email protected]

+2001003040898

Sponsors and collaborators

Lead sponsor

Assiut University

Other

Registry information

Important dates

Study start
2025
Primary completion
2027
Study completion
2027
First posted
Dec 29, 2025
Registry last updated
Dec 29, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.