Clinical Trials Directory

Trials / Completed

CompletedNCT01248000

The Use of FDG-PET in Patient With Hodgkin Lymphoma: a Population Based Study From Northern Italy

The Use of FDG Positron Emission Tomography (PET)in Patient With Hodgkin Lymphoma (HL) in the "Real World": a Population Based Study From Northern Italy

Status
Completed
Phase
Study type
Observational
Enrollment
136 (actual)
Sponsor
Gruppo Italiano Studio Linfomi · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

Positron Emission Tomography (PET) represents a step forward in the definition of response to therapy in patients with Hodgkin Lymphoma (HL). In particular the use of PET for the early assessment of response has been described as the most important tool for predicting the risk of disease progression. As no data are available to support the use of early assessment of response for adapting and modifying subsequent treatment, the use of PET should be limited only to patients enrolled in clinical trials. Irrespective of recommendations PET scanning is included in the current management of patients with HL at baseline, mid treatment, end of treatment, and follow-up. So far no study has been performed to verify how PET is currently used in the clinical setting and to assess if and how results of PET scanning are used for supporting treatment and clinical decisions.

Conditions

Interventions

TypeNameDescription
PROCEDUREFDG-PETPET interpretation is based on a site-to-site comparison of FDG uptake both before and after chemotherapy (qualitative approach), according to the criteria defined by Cheson (2008)

Timeline

Start date
2009-05-01
Completion
2010-05-01
First posted
2010-11-25
Last updated
2010-11-25

Locations

1 site across 1 country: Italy

Source: ClinicalTrials.gov record NCT01248000. Inclusion in this directory is not an endorsement.