Characterization of Abdomino-pelvic Lesions by 18Fluorine- Fluorodeoxyglucose Positron Emission Tomography/Computed Tomography

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
AgeNot listed
SponsorAssiut University

About this trial

The aim of the study is to identify and characterize lesions in the abdominopelvic region detected by 18fluorine- fluorodeoxyglucose (FDG) positron Emission Tomography combined Computed Tomography (PET/CT) scan, including determining their malignant or benign nature, and to determine the extent of disease to facilitate proper management

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Inclusion criteria: All of the patients were suspected of having malignancy (new, recurrent or metastatic) based on pathology or conventional radiological studies and were referred to nuclear medicine unit for 18F-FDG-PET-CT scan

Disqualifiers

patients underwent recent abdominal or pelvic surgery.

patients with blood glucose level ˃200 mg/dL

Pregnancy

Trial population

patients were suspected of having malignancy (new, recurrent or metastatic) based on pathology or conventional radiological studies and were referred to nuclear medicine unit for 18F-FDG-PET-CT scan

Trial design

Design model

Other

Time perspective

Cross-sectional

Treatments tested in this trial

  • PET/CT

    Device

    positron emission tomography/computed tomography

Treatment groups

No treatment groups listed

Trial outcomes

Primary outcomes

1

Evaluate the performance of 18F FDG PET/CT

identify and characterize abdominopelvic lesions, initial staging, follow up of treatment and detection of recurrence in the abdominopelvic region, including determining their malignant or benign nature, and to determine the extent of disease, Assess the spread of disease to lymph nodes, distant metastases, or other areas, to facilitate proper management.

Time frame
3 years

Secondary outcomes

1

Evaluate the diagnostic power of alternative technologies

Evaluate the diagnostic power of alternative technologies like dual time point images, bladder evacuation and forced diuresis in characterizing abdominopelvic lesions.

Time frame
3 years

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

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