Trial Information
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
Inclusion Criteria:
1. Histologically confirmed classical Hodgkin lymphoma according to the current World
Health Organisation Classification (nodular sclerosis, mixed cellularity, lymphocyte
rich, lymphocyte depleted).
2. Clinical stage I-IV.
3. No previous chemotherapy, radiotherapy or other investigational drug for HL.
Exclusion Criteria:
1. None.
Type of Study:
Observational
Study Design:
Observational Model: Cohort, Time Perspective: Retrospective
Outcome Measure:
Progression-free survival
Outcome Time Frame:
within 1 month after end of treatment
Safety Issue:
No
Principal Investigator
Massimo Federico, MD
Investigator Role:
Study Chair
Investigator Affiliation:
Università di Modena e Reggio Emilia
Authority:
Italy: Ethics Committee
Study ID:
PET-LH
NCT ID:
NCT01248000
Start Date:
May 2009
Completion Date:
May 2010
Related Keywords:
- Histologically Confirmed Classical Hodgkin Lymphoma According to the Current World Health Organisation Classification
- Hodgkin lymphoma
- FDG-PET
- prognostic factor
- clinical trial
- Hodgkin Disease
- Lymphoma