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LIFSCREEN : Evaluation of Whole Body MRI for Early Detection of Cancers in Subjects With P53 Mutation (Li-Fraumeni Syndrome)

Basic Trial Information
Trial Description
     Summary
     Eligibility Criteria
Trial Contact Information

Basic Trial Information

PhaseTypeStatusAgeSponsorProtocol IDs
Phase IIIScreeningActive5 to 71OtherCSET2011/1748
NCT01464086

Trial Description

Summary

The purpose of this study is to compare the diagnostic efficacy of two follow-up schedules for the early detection of cancers in the population under study on cancer incidence at 3 years.

Eligibility Criteria

Inclusion Criteria:

  • P53 mutation

Trial Contact Information

Trial Lead Organizations/Sponsors

Institut Gustave Roussy

Olivier caronPh: 33 1 42 11 51 78
  Email: olivier.caron@igr.fr

Trial Sites

France
  Villejuif
 Institut Gustave Roussy
 Olivier caron Ph: 33 1 42 11 51 78

Link to the current ClinicalTrials.gov record.
NLM Identifer NCT01464086
Information obtained from ClinicalTrials.gov on December 14, 2011

Note: Information about this trial is from the ClinicalTrials.gov database. The versions designated for health professionals and patients contain the same text. Minor changes may be made to the ClinicalTrials.gov record to standardize the names of study sponsors, sites, and contacts. Cancer.gov only lists sites that are recruiting patients for active trials, whereas ClinicalTrials.gov lists all sites for all trials. Questions and comments regarding the presented information should be directed to ClinicalTrials.gov.

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