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Personalised Program for Women Treated for Hodgkin Disease

Basic Trial Information
Trial Description
     Summary
     Eligibility Criteria
Trial Contact Information

Basic Trial Information

PhaseTypeStatusAgeSponsorProtocol IDs
No phase specifiedScreeningActive18 and overOtherPROPER/IPC 2010-001
NCT01188915

Trial Description

Summary

After treatment for Hodgkin disease, secondary cancer, in particular breast cancer induced by treatment, are the first cause of death.

The investigators will estimate the risk to develop breast cancer in this population of women treated for hodgkin disease, and will propose women at high rish to participate in an intensive screening program based on an annual detection based on mammography, echography, and RMI.

Eligibility Criteria

Inclusion Criteria:

  • women > 18 years
  • treated for Hodgkin disease
  • signed informed consent
  • high risk of breast cancer

Exclusion Criteria:

  • patients unable to have a regular follow-up

Trial Contact Information

Trial Lead Organizations/Sponsors

Marseille Institute of Cancer - Institut J. Paoli and I. Calmettes

F. EisingerPrincipal Investigator

Dominique GENRE, MDPh: (33) 4 91 22 37 78
  Email: bec@marseille.fnclcc.fr

Trial Sites

France
  Marseille
 François EISINGER, PhD

Link to the current ClinicalTrials.gov record.
NLM Identifer NCT01188915
Information obtained from ClinicalTrials.gov on May 29, 2012

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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