Comparison Between FDG-PET and MRI for the Assessment of Response to Intensive Chemotherapy in Multiple Myeloma Patients.

NCT00200668 · Status: TERMINATED · Phase: NA · Type: INTERVENTIONAL

Last updated 2008-06-09

No results posted yet for this study

Summary

Comparison between FDG-PET and MRI for the assessment of response to intensive chemotherapy in multiple myeloma patients.

Conditions

Interventions

DRUG

FDG = fluorodeoxyglucose

Sponsors & Collaborators

  • Nantes University Hospital

    lead OTHER

Principal Investigators

  • Olivier Couturier, MD · Nantes University Hospital

Study Design

Allocation
NON_RANDOMIZED
Purpose
DIAGNOSTIC
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Max Age
65 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2005-03-31
Completion
2006-12-31

Countries

  • France

Study Locations

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00200668 on ClinicalTrials.gov