Clinical Trials Directory

Trials / Withdrawn

WithdrawnNCT01789892

Methylprednisolone Before Fludeoxyglucose-Labeled Positron Emission Tomography in Patients With Lung Cancer

FDG PET/CT: Reducing False Positive Mediastinal Uptake by Premedicating With Methylprednisolone

Status
Withdrawn
Phase
N/A
Study type
Interventional
Enrollment
0 (actual)
Sponsor
Ohio State University Comprehensive Cancer Center · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to determine whether giving an anti-inflammatory medication (corticosteroid) prior to a positron emission tomography scan (PET) scan may reduce or eliminate false findings related to inflammation

Detailed description

PRIMARY OBJECTIVES: I. To assess whether premedication with a corticosteroid may reduce false positive findings on fluorodeoxyglucose (fludeoxyglucose F 18 \[FDG\[) PET/computed tomography (CT) scans in lung cancer patients, by reducing radiotracer uptake in thoracic lymph nodes related to inflammation. OUTLINE: Within 1-14 days of undergoing standard FDG PET/CT scan, patients receive methylprednisolone intravenously (IV) and then undergo a second FDG PET/CT scan. After completion of study treatment, patients are followed up for 2 years.

Conditions

Interventions

TypeNameDescription
DRUGmethylprednisoloneGiven IV
RADIATIONfludeoxyglucose F 18Undergo FDG PET/CT scan
PROCEDUREpositron emission tomographyUndergo FDG PET/CT scan
PROCEDUREcomputed tomographyUndergo FDG PET/CT scan

Timeline

Start date
2011-06-01
Primary completion
2013-01-01
Completion
2013-01-01
First posted
2013-02-12
Last updated
2018-06-28

Source: ClinicalTrials.gov record NCT01789892. Inclusion in this directory is not an endorsement.