Clinical Trials Directory

Trials / Completed

CompletedNCT00712556

PET Study in Patients With Non-Hodgkin Lymphoma

Positron Emission Tomography Study in Patients With Non-Hodgkin Lymphoma

Status
Completed
Phase
Study type
Observational
Enrollment
55 (actual)
Sponsor
Vanderbilt-Ingram Cancer Center · Academic / Other
Sex
All
Age
Healthy volunteers
Not accepted

Summary

RATIONALE: Diagnostic procedures, such as fluorine 18-fludeoxyglucose positron emission tomography (PET) scans, may help doctors predict a patient's response to treatment and help plan the best treatment. PURPOSE: This phase I trial is studying fluorine 18-fludeoxyglucose PET scan to see how well it predicts outcomes in patients who have undergone high-dose chemotherapy and autologous stem cell transplant for non-Hodgkin lymphoma.

Detailed description

OBJECTIVES: * To determine if a fluorine 18-fludeoxyglucose positron emission tomography scan, performed as early as day 30 after high-dose chemotherapy and autologous stem cell transplantation, may be useful in identifying patients with non-Hodgkin lymphoma who may benefit from early interventions, including reduced intensity stem cell transplantation or additional therapy, to preempt disease relapse and improve overall survival. OUTLINE: Conventional imaging, biopsy, and clinical examination findings are reviewed to determine patient clinical outcome (e.g., complete remission, disease progression/relapse, or death related to the primary disease).

Conditions

Interventions

TypeNameDescription
RADIATIONfluorine 18-fludeoxyglucose positron emission tomographyfluorine 18-fludeoxyglucose is a radioactive isotope used in PET to detect cancer tumors

Timeline

Start date
2008-05-01
Primary completion
2009-03-01
Completion
2009-03-01
First posted
2008-07-10
Last updated
2013-02-26

Locations

3 sites across 1 country: United States

Source: ClinicalTrials.gov record NCT00712556. Inclusion in this directory is not an endorsement.