Comparison of NaF PET-CT and Diffusion MRI in the Diagnosis of Bone Metastases (IMMETAOS)

Sponsor
Institut Jean-Godinot (Other)
Overall Status
Completed
CT.gov ID
NCT02876731
Collaborator
(none)
13
1
23

Study Details

Study Description

Brief Summary

Prospective, monocentric, comparative, non randomised

Primary objective :
  • to compare the diagnostic accuracy of sodium fluoride PET-CT and MRI using the conventional block and diffusion sequence in the search for bone metastases
Secondary objectives :
  • compare accuracy of MRI diffusion and conventional MRI

  • explore the evolution of the results of the different types of imaging over time or under treatment for patients with repeated examinations at 6 months

Condition or Disease Intervention/Treatment Phase
  • Device: PET-CT
  • Device: MRI
N/A

Detailed Description

Prospective, monocentric, comparative, non randomised.

Organization of NaF PET-CT and MRI on the same day or within a 10 days period.

At 6 months :
  • repeat both exams systematically if one of the initial tests showed a suspicious or doubtful abnormality

  • final diagnosis by a committee of practitioners using the whole patient's file

Scheduled Project inclusion duration of 36 months (possible adaptation of duration in order to obtain the number of required patients)

Study Design

Study Type:
Interventional
Actual Enrollment :
13 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Diagnostic
Official Title:
Comparison of NaF PET-CT and Diffusion MRI in the Diagnosis of Bone Metastases
Study Start Date :
Jul 1, 2013
Actual Primary Completion Date :
Jun 1, 2015
Actual Study Completion Date :
Jun 1, 2015

Arms and Interventions

Arm Intervention/Treatment
Other: single group

PET-CT MRI

Device: PET-CT
NaF PET-CT

Device: MRI
DWMRI

Outcome Measures

Primary Outcome Measures

  1. Evidence of Bone metastasis according to a clinician and imaging practitionners group based on clinical and imaging evolution [Up to 38 months]

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Man or woman over 18 years

  • Osteophilic cancer (breast, prostate, lung, kidney, thyroid) proved by pathological material, with a high probability of bone metastases

  • With an indication to a bone examination: systematic search for metastasis for the staging or due to clinical or laboratory suspicion of bone metastasis

  • Registered in a social security health scheme

  • Written informed consent obtained

Exclusion Criteria:
  • Classical contra-indications for PET CT (suspected pregnancy) or MRI (pacemaker, ferromagnetic material); for patients with a possibility of pregnancy (women of childbearing age without contraception and second part of the menstrual cycle, or the slightest suspicion), verification of the absence of pregnancy will be made by the beta HCG dosage before injection of radioactive tracer

  • Uncontrollable claustrophobia with treatment anxiolytic

  • Antitumor treatment started between the two imaging tests

  • Imaging or treatment needed in emergency, if both tests are not performable in time required for the care

  • Inaugural neurological complication

  • Patient unable to undergo biomedical research (under guardianship or deprived of liberty)

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

  • Institut Jean-Godinot

Investigators

  • Study Director: Yacine MERROUCHE, Institut Jean-Godinot

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Institut Jean-Godinot
ClinicalTrials.gov Identifier:
NCT02876731
Other Study ID Numbers:
  • 2012-A00381-42
First Posted:
Aug 24, 2016
Last Update Posted:
Aug 24, 2016
Last Verified:
Aug 1, 2016
Individual Participant Data (IPD) Sharing Statement:
Undecided
Plan to Share IPD:
Undecided
Additional relevant MeSH terms:

Study Results

No Results Posted as of Aug 24, 2016